Abstract
The house mouse has emerged as the laboratory animal par excellence for mammalian genetics. The main reason for this is technical but there is also the fact that the mouse ‘got in first’ in those early days when the variations present in fanciers’ stocks were eagerly exploited for confirmation and extension of Mendelian inheritance. This early lead has never been lost and the accumulative information on the species is now so extensive that no other mammalian species is likely to supplant it. This is not to imply that the house mouse is ideal for all types of research, nor that the comparative genetics of other species should be neglected. Far from it in fact. Excessive concentration on one species is to be deplored.
This is a preview of subscription content, log in via an institution to check access.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Preview
Unable to display preview. Download preview PDF.
Bibliography
ABEELEN, J. H. F., Van and KROON, P. H. W., Van der (1967). Nijmegen waltzer, a new neurological mutant in the mouse. Genet. Res., 10, 117–118.
ALLEN, S. L. (1955a). H-2 f, a tenth allele in the histocompatibility locus in the mouse as determined by tumour transplantation. Cancer Res., 15, 315–319.
ALLEN, S. L. (1955b). Linkage relations of the genes histocompatibility-2 and fused tail, brachyury and kinky tail in the mouse, as determined by transplantation. Genetics, 40, 627–650.
AMAND, W. St. (1970). Recombination frequency estimates for the satin-beige interval in the mouse. J. Miss. Acad. Sci., 15, 60.
AMOS, A. B., GOVER, P. A. and MIKULSKA, Z. B. (1955). An analysis of an antigenic system in the mouse (the H-2 system). Proc. Roy. Soc. B., 144, 369–380.
AMOS, D. B., ZUMPFT, M. and ARMSTRONG, P. (1963). H-5 and H-6, two mouse isoantigens on red cells and tissues detected serologically. Transplantation, 1, 270.
AUERBACH, C., FALCONER, D. S., and ISAACSON, J. H. (1962). Test for sex-linked lethals in irradiated mice. Genet. Res., 3, 444–447.
BAILEY, D. W. (1962). Histocompatibility associated with the X chromosome in mice. Genetics, 47, 9–39.
BAILEY, D. W. (1963a). Histocompatibility associated with the X chromosome in mice. Transplantation, 1, 70–74.
BAILEY, D. W. (1963b). Mosaic histocompatibility of skin grafts from female mice. Science, 141, 631–633.
BAILEY, D. W. (1964). Genetically modified survival time of grafts from mice bearing X linked histocompatibility. Transplantation, 2, 203–206.
BAILEY, D. W. (1965). A search for genetic background influences on survival time of skin grafts from mice bearing Y linked histocompatibility. Transplantation, 3, 531–534.
BATEMAN, N. (1961). Sombre, a viable dominant mutant in the house mouse. J. Hered., 52, 186–189.
BEATTY, R. A. (1957). Chromosome constancy in the corneal epithelium of the mouse. Chromosoma, 8, 585–596.
BECK, S. L. (1963). The anophthalmic mutant of the mouse, II. An association of anophthalmia and polydactyly. J. Hered., 54, 79–83. BENNETT, D. (1959). Brain hernia, a near recessive mutation in the house mouse. J. Hered., 50, 265–268.
BENNETT, D. (1965). The karyotype of the mouse, with identification of a translocation. Proc. Nat. Acad. Sci. U.S.A., 53, 730–737.
BENNETT, D. (1966). Non-random association of chromosomes during mitotic metaphase in tissue cells of the mouse. Cytologia, 31, 411–415.
BENNETT, J. H. and GRESHAM, G. A. (1956). A gene for eyelids open at birth in the house mouse. Nature, 178, 272–273.
BERNSTEIN, S. E., SILVERS, A. A. and SILVERS, W. K. (1958). An attempt to demonstrate a Y linked histocompatibility gene in the house mouse. J. Nat. Cancer Inst., 20, 577.
BIDDLE, F. G. and PETRAS, M. L. (1967). The inheritance of a non-hemoglobin protein in Mus musculus. Genetics, 57, 943–949.
BILLINGHAM, R. E. and SILVERS, W. K. (1960). Studies on tolerance of the Y chromosome antigen in mice. J. Immunol., 85, 14–26.
BILLINGHAM, R. E. and SILVERS, W. K. (1963). Sensitivity to homografts of normal tissues and cells. Ann. Rev. MicrobioL, 17, 531–564.
BITTNER, J. J. (1934). Linkage in transplantable tumours. J. Genet., 29, 17–27.
BLOOM, J. L. (1961). Pulmonary tumours and group VII in the mouse. Nature, 191, 1124–1125.
BLOOM, J. L. and FALCONER, D. S. (1966). Grizzled, a mutant in linkage group X of the mouse. Genet. Res., 7, 159–167.
BODNER, W. F. (1961a). Viability effects and recombination differences in a linkage test with pallid and fidget in the house mouse. Heredity, 16, 485–495.
BODNER, W. F. (1961b). Effects of maternal age on the incidence of congenital abnormalities in mouse and man. Nature, 190, 1134–1135.
BORGER, R. (1950), Order of genes on the fifth linkage group of the house mouse. Nature, 166, 697.
BOYSE, E. A., MIYAZAWA, M., AOKI, T. and OLD, L. J. (1968). Ly-A and Ly-B: two systems of lymphocyte isoantigens in the mouse. Proc. Roy. Soc. Lond., B, 170, 175–193.
BOYSE, E. A., OLD, L. J. and LUELL, S. (1964). Genetic determination of the TL (thymus-leukemia) antigen in the mouse. Nature, 201, 779.
BRYSON, V. (1944). Spermatogenesis and fertility in Mus musculus as affected by factors at the T locus. J. Morph., 74, 131–179.
BUNKER, H. and SNELL, C. D. (1948). Linkage of white and waved-1. J. Hered., 39, 28.
BUNKER, L. E. (1959). Hepatic fusion, a new gene in linkage group I of the mouse. J. Hered., 50, 4044.
BUNKER, M. C. (1961). A technique for straining chromosomes of the mouse with Sudan Black B. Canad. J. Genet. Cytol., 3, 355–360.
BUNKER, M. C. (1965). Chromosome preparations from solid tumours of the mouse: a direct method. Canad. J. Genet. CytoL, 7, 78–83.
BURHOE, S. O. (1936). Linkage studies of waved coat in the house mouse. J. Hered., 27, 119–120.
CACHEIRO, N. L. A. and RUSSELL, L. B. (1969). Cytological studies of X-autosomal translocations in the mouse. I. Mitotic chromosomes. Genetics, 61, 58.
CARTER, T. C. (1947). A new linkage in the house mouse: undulated and agouti. Heredity, 1, 367–372.
CARTER, T. C. (1949). Position of luxate in the third linkage group of the house mouse. Nature, 164, 11–38.
CARTER, T. C. (1951a). The position of fidget in linkage group V of the house mouse. J. Genet., 50, 264–267.
CARTER, T. C. (195 lb). Wavy coated mice: phenotypic interactions and linkage tests between rex and (a) waved-1, (b) waved-2. J. Genet., 50, 277–299.
CARTER, T. C. (1951c). The genetics of luxate mice. II. Linkage and independence. J. Genet., 50, 300–306.
CARTER, T. C. (1954). A search for chromatid interference in the male house mouse. Z. Ind. Abst. Vererbgslehre, 86, 210–223.
CARTER, T. C. (1955). The estimation of total genetic map lengths from linkage test data. J. Genet., 53, 21–28.
CARTER, T. C. (1956). Genetics of the Little and Bagg X-rayed mouse stock. J. Genet., 54, 311–326.
CARTER, T. C. (1957). The use of linked marker genes for detecting recessive autosomal lethals in the mouse. J. Genet., 55, 585–597.
CARTER, T. C. and FALCONER, D. S. (1951). Stocks for detecting linkage in the mouse and the theory of their design. J. Genet., 50, 307–323.
CARTER, T. C. and FALCONER, D. S. (1952). A review of independent segregation in the house mouse. J. Genet., 50, 399–413.
CARTER, T. C. and FALCONER, D. S. (1953). Independence of linkage groups I, II, and XI in the house mouse. J. Genet., 51, 373–374.
CARTER, T. C. and GRUNEBERG, H. (1950). Linkage between fidget and agouti in the house mouse. Heredity, 4, 373–376.
CARTER, T. C., LYON, M. F. and PHILLIPS, R. J. S. (1954). Partial sex linkage in the mouse. Nature, 174, 309–310.
CARTER, T. C., LYON, M. F. and PHILLIPS, R. J. S. (1955). Gene tagged chromosome translocations in eleven stocks of mice. J. Genet., 53, 154–166.
CARTER, T. C., LYON, M. F. and PHILLIPS, R. J. S. (1956). Further genetic studies of eleven translocations in the mouse. J. Genet., 54, 462–473.
CARTER, T. C. and PHILLIPS, R. J. S. (1953). The sex distribution of waved-2, shaker-2 and rex in the house mouse. Z. Ind. Abst. Vererbgslehre, 85, 564–578.
CARTER, T. C. and PHILLIPS, R. J. S. (1954). Ragged, a semidominant coat texture mutant in the house mouse. J. Hered., 45, 150–154.
CASTLE, W. E. (1919). Studies of heredity in rabbits, rats and mice. Car. Inst. Wash. Pub., 288, 56 pp.
CASTLE, W. E. (1925). A sex difference in linkage in rats and mice. Genetics, 10, 580–582.
CASTLE, W. E. (1941). Influence of certain colour mutations on body size in mice, rats and rabbits. Genetics, 26, 177–191.
CASTLE, W. E., GATES, W. H. and REED, S. C. (1936). Studies of a size cross in mice. Genetics, 21, 66–78.
CASTLE, W. E., GATES, W. H., REED, S. C. and LAW, L. W. (1936). Studies of a size cross in mice II. Genetics, 21, 310–323.
CASTLE, W. E., GATES, W. H., REED, S. C. and SNELL, G. D. (1936). Identical twins in a mouse cross. Science, 84, 581.
CASTLE, W. E. and LITTLE, C. C. (1909). The peculiar inheritance of pink eyes among coloured mice. Science, 30, 313–314.
CASTLE, W. E. and WACHTER, W. L. (1924). Variations of linkage in rats and mice. Genetics, 9, 1–12.
CATTANACH, B. M. (1961a). XXY mice. Genet. Res., 2, 156–158. CATTANACH, B. M. (1961b). A chemically induced variegated type position effect in the mouse. Z. Veverbungslehre, 92, 165–182.
CATTANACH, B. M. (1962). XO mice. Genet. Res., 3, 487–490.
CATTANACH, B. M. (1964). Autosomal trisomy in the mouse. Cytogenetics, 3, 159–166.
CATTANACH, B. M. (1965). Snaker: a dominant abnormality caused by chromosomal imbalance. Z. Vererbungslehre, 96, 275–284.
CATTANACH, B. M. (1966). The location of Cattanach’s translocation in the X chromosome linkage of the mouse. Genet. Res., 8, 253–256.
CATTANACH, B. M. (1967). A test of distributive pairing between two specific non-homologous chromosomes in the mouse. Cytogenetics, 6, 67–7 7.
CATTANACH, B. M. and ISAACSON, J. H. (1967). Controlling elements in the mouse X chromosome. Genetics, 57 331.
CATTANACH, B. M., PEREZ, J. N. and POLLARD, C. E. (1970). Controlling elements in the mouse X chromosome. II. Location in the linkage map. Genet. Res., 15, 183–195.
CATTANACH, B. M. and POLLARD, C. E. (1969). A XYY sex chromosome constitution in the mouse. Cytogenetics, 8, 80–86.
CATTANACH, B. M., POLLARD, C. E. and PEREZ, J. N. (1969). Controlling elements in the mouse X chromosome. I. Interaction with the X linked genes. Genet. Res., 14, 223–235.
CELADA, F. and WELSHONS, W. J. (1963). An immunogenetic analysis of the male antigen in mice utilising animals with an exceptional chromosome constitution. Genetics, 48, 139–151.
CENTER, E. M. (1966). Genetical and embryological studies of the jt form of syndactylism in the mouse. Genet. Res., 8, 33–40.
CHANG, S. S. and HILDEMANN, W. H. (1964). Inheritance of susceptibility to polyoma virus in mice. J. Nat. Cancer Inst., 33, 303–313.
CHASE, H. B. (1946). A sex-linked recessive in the mouse. Genetics, 31, 214.
CHU, E. H. Y. and MONESI, V. (1960). Analysis of X-ray.induced chromosome aberrations in mouse somatic cells in vitro. Genetics 45, 981.
CINADER, B., DUBISKI, S. and WARDLAW, A. C. (1966). Genetics of MuBI and a complement effect in inbred strains of mice. Genet. Res., 7, 32–43.
CLARK, F. H. (1934a). Linkage studies of brachyury in the house mouse. Proc. Nat. Acad. Sci., U.S.A., 20, 276–279.
CLARK, F. H. (1934b). The inheritance and linkage relations of a new recessive spotting in the house mouse. Genetics, 19, 365–393.
CLARK, F. H. (1935). Linkage relations of Zavadskaia shaker in the house mouse. Proc. Nat. Acad. Sci. U.S.A., 21, 247–251.
CLARK, F. H. (1936). Linkage relations of hydrocephalus-1 in the house mouse. Proc. Nat. Acad. Sci. U.S.A., 22, 474–478.
CLOUDMAN, A. M. and BUNKER, L. E. (1945). The varitint-waddler mouse. J. Hered., 36, 258–263.
COHEN, B. L. (1960). Genetics of plasma transferrius in the mouse. Genet. Res., 1, 431–438.
COLLINS, R. L. (1970). A new genetic locus papped from behavioural variation in mice: audiogenic siezure prone (asp) Behay. Genet., 1, 99–109.
COLLINS, R. L. and FULLER, J. L. (1968). Audiogenic seizure prone: a gene affecting behaviour in linkage group VIII of the mouse. Science, 162, 1137–1139.
COLLINS, R. L. and HUTTON, J. J. (1970). The position of autosomal glucose-6-phosphate dehydrogenase on linkage group VIII of the mouse. J. Hered., 61, 53–54.
COOPER, C. B. (1939). Linkage between naked and caracul in the house mouse. J. Hered., 30, 212.
COX, E. K. (1926). The chromosomes of the house mouse. J. Morph., 43, 45–54.
CREW, F. A. E. and AUERBACH, C. (1939). Rex: a dominant autosomal monogenic coat texture character in the mouse. J. Genet., 38, 341–344.
CREW, F. A. E. and AUERBACH, C. (1940). Linkage date on the rex character in the house mouse. J. Genet., 39, 225–227.
CREW, F. A. E. and KOLLER, P. C. (1932). The sex incidence of chiasma frequency and genetic crossingover in the mouse. J. Genet., 26, 359–383.
CRIPPA, M. (1964). The mouse karyotype in somatic cells cultured in vitro. Chromosoma, 15, 301–311.
CURRY, G. A. (1959). Genetic and developmental studies on droopy eared mice. J. Embryol. Exp. Morph., 7, 39–65.
CUTWRIGHT, P. R. (1932). The spermatogenesis of the mouse. J. Morph., 54, 197–220.
DARBISHIRE, A. D. (1904). On the result of crossing Japanese waltzing with albino mice. Biometrika, 3, 1–51.
DAVID, C. S., SHREFFLER, D. C. and STIMPFLING, J. H. (1969) Analysis of four crossovers within the complex H-2 region of the house mouse. Genetics, 61, 12–13.
DE LORENZO, R. J. and RUDDLE, F. H. (1969). Genetic control of two electrophoretic variants of glucosephosphate isomerase in the mouse. Biochem. Genet., 3, 151–162.
DEOL, M. S. and GREEN, M. C. (1966). Snell’s waltzer, a new mutation affecting behaviour and the inner ear in the mouse. Genet. Res., 8, 339–345.
DEOL, M. S. and LANE, P. W. (1966). A new gene affecting the morphogenesis of the vestibular part of the inner ear in the mouse. J. Embryol. Exp. Morph., 16, 543–558.
DEOL, M. S. and ROBINS, M. W. (1962). The spinner mouse. J. Hered., 53, 133–136.
DETLEFSEN, J. A. (1925). Linkage of dark-eye and color in mice. Genetics, 10, 17–32.
DETLEFSEN, J. A. and CLEMENTE, L. S. (1924). Linkage of a dilute color factor and dark-eye in mice. Genetics, 9, 247–260.
DETLEFSEN, J. A. and ROBERTS, E. (1918). On a backcross in mice involving three allelomorphic pairs of characters. Genetics, 3, 573–598.
DETLEFSEN, J. A. and ROBERTS, E. (1923). Linkage Studies in mice. Anat. Rec., 24, 417.
DICKERMAN, R. C., FEINSTEIN, R. N. and GRAHM, D. (1968). Position of the acatalasemia gene in linkage group V of the mouse. J. Hered., 59, 177–178.
DICKIE, M. M. (1954a). The tortoiseshell house mouse. J. Hered., 45, 158, 190.
DICKIE, M. M. (1954b). The expanding knowledge of the genome in the mouse. J. Nat. Cancer Inst., 15, 679–684.
DICKIE, M. M. (1955). Alopecia, a dominant mutation in the house mouse. J. Hered., 46, 30–34.
DICKIE, M. M. (1964). New Splotch alleles in the mouse. J. Hered., 55, 97–101.
DICKIE, M. M., KELTON, D. E., FIELDER, J. H., INGALLS, A. M. and SNELL, G. D. (1949). New mutations and linkage studies in the house mouse. Anat. Rec., 105, 540.
DICKTE, M. M. and WOOLLEY, G. W. (1946). Linkage studies with the pirouette gene in the mouse. J. Hered., 37, 335–337.
DICKIE, M. M. and WOOLLEY, G. W. (1948). Location of the pirouette gene in Mus musculus. J. Hered., 39, 288.
DICKIE, M. M. and WOOLLEY, G. W. (1950). Fuzzy mice. J. Hered., 41, 193–196.
DIPAOLO, J. A. and NOELL, W. K. (1962). Some genetic aspects of visual cell degeneration in mice. Exp. Eye Res., 1, 215–220.
DOUGLAS, L. T. (1966). Meosis. I. Association of non-homologous bivalents during spermatogenesis in white mice. Genetica, 37, 466–480.
DOUGLAS, L. T. and GEERTS, S. J. (1966). Meiosis. II. A modified affinity model in mice. Genetica, 37, 511–542.
DRAY, S., LIEBERMAN, R. and HOFFMAN, H. A. (1963). Two murine gamma-globulin allotypic specifities identified by ascitic fluid isoprecipitins and determined by allelic genes. Proc. Soc. Exp. Biol. Med., 113, 509.
DRAY, S. POTTER, M. and LIEBERMAN, R. (1965). Immunochemical and genetic studies of two distinct gamma-G-immunoglobulins in BALB/C mice. J. Immunolog., 95, 823–833.
DUNN, L. C. (1919). Anomalous ratios in a family of yellow mice suggesting linkage between the genes for yellow and for black. Amer. Nat., 53, 558–560.
DUNN, L. C. (1920a). Linkage in mice and rats. Genetics, 5, 325–343.
DUNN, L. C. (1920b). Independent genes in mice. Genetics, 5, 344–361.
DUNN, L. C. (1920c). Types of white spotting in mice. Amer. Nat., 54, 465–495.
DUNN, L. C. (1945). A new eye. color mutant in the mouse with asymmetrical expression. Proc. Nat. Acad. Sci. U.S.A., 31, 343–346.
DUNN, L. C. (1956). Analysis of a complex gene in the house mouse. Cold Spring Harb. Symp. Quant. Biol., 21, 187–195.
DUNN, L. C. and BENNETT, D. (1968). A new case of transmission ratio distortion in the house mouse. Proc. Nat. Acad. Sci. U.S.A., 61, 570–573.
DUNN, L. C., BENNETT, D. and BEASLEY, A. B. (1962). Mutation and recombination in the vicinity of a complex gene. Genetics, 47, 285–303.
DUNN, L. C. and CASPARI, E. (1942). Close linkage between mutations with similar effects. Proc. Nat. Acad. Sci. U.S.A., 28, 205–210.
DUNN, L. C. and CASPARI, E. (1945). A case of neighbouring loci with similar effects. Genetics, 30, 543–568.
DUNN, L. C. and GLUECKSOHN—SCHOENHEIMER, S. (1939). The inheritance of taillessness (anury) in the house mouse. II. Taillessness in a second balanced line. Genetica, 24, 587–609.
DUNN, L. C. and GLUECKSOHN—SCHOENHEIMER, S. (1943). Tests for recombination among three lethal mutations in the house mouse. Genetics, 28, 29–40.
DUNN, L. C. and GLUECKSOHN-SCHOENHEIMER, S. (1950). Repeat mutations in one area of a mouse chromosome. Proc. Nat. Acad. Sci. U.S.A., 36, 233–237.
DUNN L. C., GLUECKSOHN-SCHOENHEIMER, S. and BRYSON, V. (1940). A new mutation in the mouse affecting spinal column and urogenital system. J. Hered., 31, 343–348.
DUNN, L. C. and GLUECKSOHN-WAELSCH, S. (1953a). Genetic analysis of seven newly discovered mutant alleles at locus T in the house mouse. Genetics, 38, 261–271.
DUNN, L. C. and GLUECKSOHN-WAELSCH, S. (1953b). The failure of a t allele to suppress crossingover in the mouse. Genetics, 38, 512–517.
DUNN, L. C. and GLUECKSOHN-WAELSCH, S. (1954). Genetical study of the mutation `fused’ in the house mouse, with evidence concerning its allelism with a similar mutation `kink’ J. Genet., 52, 383–391.
DURHAM, F. M. (1908). A preliminary account of the inheritance of coat colour in mice. Rep. Evol, Commit. Roy. Soc., 4, 41–53.
DURHAM, F. M. (1911). Further experiments on the inheritance of coat colour in mice. J. Genet., 1, 159–178.
EGOROV, I. K. (1965). A new isoantigen of mouse erythrocytes. Genetika, Mosk., 1965 (6), 80–85.
EICHER, E. M. (1967). The genetic extent of the insertion involved in the flecked translocation in the mouse. Genetics, 55, 203–212.
EICHER, E. M. (1970a). The position of ru-2 and qv with respect to the flecked translocation in the mouse. Genetics, 64, 495–510.
EICHER, E. M. (1970b). X-autosomal translocations in the mouse: total inactivation versus partial inactivation of the X chromosome. Advanc. Genet., 15, 175–259.
EICHWALD, E. J., DAVIDSON, N. and MOORE, M. (1966). The murine Y chromosome as a marker. Transplantation, 4, 332–333.
EICHWALD, E. J. and SILMSER, C. R. (1955). Untitled communication. Transpl. Bull., 2, 148–149.
EICHWALD, E. J., SILMSER, C. R. and WEISSMAN, I. (1958). Sex-linked rejection of normal and neoplastic tissue. I. Distribution and specificity. J. Nat. Cancer Inst., 20, 563–575.
EICHWALD, E. J., SILMSER, C. R. and WHEELER, N. (1957). The genetics of skin grafting. Ann. N.Y. Acad. Sci., 64, 737–740.
ERICKSON, R. P., GLUECKSOHN-WAELSCH, S. and CORI, C. F. (1968). Glucose-6-phosphatase deficiency caused by radiation induced alleles at the albino locus in the mouse. Proc. Nat. Acad. Sci. U.S.A., 59, 437–444.
EPSTEIN, C. J. (1969). Mammalian oocytes: X chromosome activity. Science, 163, 1078–1079.
EVANS, E. P., FORD, C. E. and SEARLE, A. G. (1969). A 39, X/41,XYY mosaic mouse. Cytogenetics, 8, 87–96.
EVANS, E. P., LYON, M. F. and DAGLISH, M. (1967). A mouse translocation giving a metacentric marker chromosome. Cytogenetics, 6, 106–119.
FALCONER, D. S. (1947). Linkage of rex with shaker-z in the house mouse. Heredity, 1, 133;135.
FALCONER. D. S. (1951). Two new mutants, trembler and reeler, with neurological actions in the house mouse. J. Genet., 50, 192–201.
FALCONER, D. S. (1952a). Location of reeler in linkage group III in the mouse. Heredity, 6, 255–257.
FALCONER, D. S. (1952b). A totally sex-linked gene in the house mouse. Nature, 169, 664–665.
FALCONER, D. S. (1953). Total sex-linkage in the house mouse. Z. Ind. Abst. Vererbgslehre, 85, 210–219.
FALCONER, D. S. (1954). Linkage in the mouse: the sex-linked genes and rough. Z. Ind. Abst. Vererbgslehre, 86, 263–268.
FALCONER, D. S. and ISAACSON, J. H. (1959). Adipose, a new inherited obesity of the mouse. J. Hered., 50, 290–292.
FALCONER, D. S. and ISAACSON, J. H. (1962). The genetics of sex-linked anemia in the mouse. Genet. R es., 3, 248–250.
FALCONER, D. S. and ISAACSON, J. H. (1966). Curly-whiskers and its linkage with tail-kinks in linkage group II of the mouse. Genet. R es., 8, 111–113.
FALCONER, D. S. and SIERTS-ROTH, U. (1951). Dreher, ein neues gen der Tanzmausgruppe bei der Hausmaus. Z. Ind. Abst. Vererbgslehre, 84, 71–73.
FALCONER, D. S., SLIZYNSKI, B. M. and AUERBACH, C. (1952). Genetical effects of nitrogen mustard in the house mouse. J. Genet., 51, 81–88.
FALCONER, D. S. and SNELL, G. D. (1952). Two new hair mutants, rough and frizzy in the mouse. J. Hered., 43, 53–57.
FALCONER, D. S. and SOBEY, W. R. (1953). The location of trembler in linkage group VII of the house mouse. J. Hered., 49, 159–160.
FELDMAN, H. W. (1924). Linkage of albino allelomorphs in rats and mice. Genetics, 9, 437–492.
FELDMAN, H. W. and PINCUS, G. (1926). On the inheritance of albinism and brown pigmentation in mice. Amer. Nat., 60, 195–198.
FELDMAN, M. (1958). The antigen determined by a Y linked histocompatibility gene. Transpl. Bull., 5, 15–16.
FIELDER, J. H. (1952). The taupe mouse. J. Hered. L43, 74–76.
FINLAYSON, J. S., HUDSON, D. M. and ARMSTRONG, B. L. (1969). Location of the Mup-a locus on mouse linkage group VIII. Genet. Res., 14, 329–331.
FISHER, R. A. (1946). A system of scoring linkage data, with special reference to the pied factors in mice. Amer. Nat., 80, 568–578.
FISHER, R. A. (1949). A preliminary linkage test with agouti and undulated mice. I. The fifth linkage group. Heredity, 3, 229–241.
FISHER, R. A. (1950a). Polydactyly in mice. Nature, 165, 407. FISHER, R. A. (1950b). Polydactyly in mice. Nature, 165, 796.
FISHER, R. A. (1953). The linkage of polydactyly with leaden in the house mouse. Heredity, 7, 91–95.
FISHER, R. A. and LANDAUER, W. (1953). Sex differences of crossingover in close linkage. Amer. Nat., 87, 116.
FISHER, R. A., LYON, M. F. and OWEN, A. R. G. (1947). The sex chromosome in the house mouse. Heredity, 1, 355–365.
FISHER, R. A. and MATHER, K. (1936a). Verification in mice of the possibility of more than fifty per cent recombination. Nature, 137, 362–363.
FISHER, R. A. and MATHER, K. (1936b). A linkage test with mice. Ann. Eugen., 7, 265–280.
FISHER, R. A. and SNELL, G. D. (1948). A twelfth linkage group in the mouse. Heredity, 2, 271–273.
FISHER, R. A. and YATES, F. (1953). Statistical tables for biological, agricultural and medical research. Edinburgh: Oliver and Boyd.
FLANAGAN, S. P. (1966). Nude, a new hairless gene with pleiotropic effects in the mouse. Genet. Res., 8, 295–309.
FLANAGAN, S. P. and ISAACSON, J. H. (1967). Close linkage between genes which cause hairlessness in the mouse. Genet. Res., 9, 99–110.
FORD, C. E. (1966). The murine Y chromosome as a marker. Transplantation, 4, 33–35.
FORD, C. E., CARTER, T. C. and HAMERTON, J. L. (1956). Cytogenetics of a mouse translocation. Heredity, 10, 284.
FORD, C. E. and EVANS, E. P. (1964). A reciprocal translocation in the mouse between the X chromosome and a short autosome. Cytogenetics, 3, 295–305.
FORD, C. E., HAMERTON, J. L., BARNES, W. H. and LOUTIT, J. F. (1956). Cytological identification of radiation chimaeras. Nature, 177, 452–454.
FORD, E. H. R. and WOLLAM, D. H. M. (1963). A study of the mitotic chromosomes of mice of the Strong A line. Exp. Cell Res., 32, 320–326.
FORSTHOEFEL, P. S. and SHENK, T. E. (1970). Linkage relations of Strong’s luxoid gene in the mouse. J. Hered., 61, 64–66.
FOSTER, M., PETRAS, M. L. and GASSER, D. L. (1968). The Ea-1 blood group locus of the house mouse: inheritance, linkage polymorphism and control of antibody synthesis. Proc. XII Inter. Congr. Genet., 1, 245.
FOX, A. S. (1958). Genetics of tissue specificity. Annals N.Y. Acad. Sci., 73, 611–634.
FRASER, A. S., SOBEY, S. and SPICER, C. C. (1953). Mottled, a sex modified lethal in the house mouse. J. Genet., 51, 217–221.
FRASER, F. C. and HERER, M. L. (1950). The inheritance and expression of the lens rupture gene in the house mouse. J. Hered, 41, 3–7.
FRASER, F. C. and SCHABTACH, G. (1962). Shrivelled: a heredity degeneration of the lens in the house mouse. Genet. Res., 3, 383–387.
FREDGA, K. (1961). Studies of the chromosomes in American obese-hyperglycaemic mice. Hereditas, 47, 615–618.
GALTON, M. and HOLT, S. F. (1965). Asynchronous replication of the mouse sex chromosomes. Exp. Cell Res., 37, 111–116.
GANSCHOW, R. and PAIGEN, K. (1967). Separate genes determining the structure and intracellular location of hepatic glucuronidase. Proc. Nat. Acad. Sci. U.S.A., 58, 938–945.
GARBER, E. D. (1952). Bent tail, a dominant sex linked mutation in the mouse. Proc. Nat. Acad. Sci. U.S.A., 38, 876–879.
GASSER, D. L. (1969). Genetic control of the immune response in mice. I. Segregation data and localization in the fifth linkage group of a gene affecting antibody production. J. ImmunoL, 103, 66–70.
GATES, W. H. (1926). The Japanese waltzing mouse. Car. Inst. Wash. Pub., 337, 83–138.
GATES, W. H. (1927a). Linkage of short ears and density in the house mouse. Proc. Nat. Acad. Sci. U.S.A., 13, 575–578.
GATES, W. H. (1927b). A case of non-disjunction in the mouse. Genetics, 12, 295–306.
GATES, W. H. (1928a). Linkage of the factors for short-ear and density in the house mouse. Genetics, 13, 170–179.
GATES, W. H. (1928b). Linkage of characters albinism and shaker in the house mouse. Anat. Rec., 41, 104.
GATES, W. H. (1929). Linkage of shaker and albinism and pink-eye in the house mouse. Anat. Rec., 44, 287.
GATES, W. H. (1931). Linkage of the factor shaker with albinism and pink-eye in the house mouse. Z. Ind. Abst. Vererbgslehre, 59, 220–226.
GATES, W. H. (1934). Linkage tests of a new shaker mutation with other factors in the house mouse. Amer. Nat., 68, 173–174.
GATES, W. H. and PULLIG, T. (1945a). Linkage of dominant white spotting with hairless in the house mouse. Genetics, 30, 4.
GATES, W. H. and PULLIG, T. (1945b). Linkage of dominant white spotting with hairless in the house mouse. Proc. La. Acad. Sci., 9, 57–60.
GEYER-DUSZYNSKA, I. (1963). On the structure of the XY bivalent in Mus musculus. Chromosoma, 13, 521–525.
GEYER-DUSZYNSKA, I. (1964). Cytological investigations on the T locus in Mus musculus. Chromosoma, 15, 478–502.
GILMAN, J. G. and SMITHIES, O. (1968). Fetal hemoglobin variants in mice. Science, 160, 885–886.
GITTES, R. F. and RUSSELL, P. S. (1961). Male histocompatibility antigens in mouse endoctrine tissues: functional and histologic evidence. J. Nat. Cancer Inst., 26, 283–303.
GLUECKSOHN-WAELSCH, S. and CORI, C. F. (1970). Glucose-6phosphatase deficiency: mechanisms of genetic control and biochemistry. Biochem. Genet., 4, 195–201.
GOLDJMAN, I. L., SMERTENKO, I. I. and VILKINA, (1966). The normal karyotype in mice of a highly leukaemic AKR strain. Byull. Eksp. Biol. Med., 61 (2), 75–78.
GOODWINS, I. R. and VINCENT, M. A. C. (1955). Further data on linkage between short-ear and maltese dilution in the house mouse. Heredity, 9, 413–414.
GORER, P. A., LYMAN, S. and SNELL, G. D. (1948). Studies on the genetic and antigenic basis of tumour transplantation. Proc. Roy. Soc. B., 135, 499–505.
GORER, P. A. and MIKULSKA, Z. B. (1959). Some further data on the H-2 system of antigens. Proc. Roy. Soc. B., 151, 57–69.
GRAHN, D., FRY, R. J. M. and HAMILTON, K. F. (1969). Genetic and pathologic analysis of the sex-linked allelic series, mottled, in the mouse. Genetics, 61, s22 - s23.
GREEN, C. V. (1931). Size inheritance and growth in a mouse species cross. III. Inheritance of adult quantitative characters. J. Exp. Zool., 59, 213–263.
GREEN, C. V. (1932). Genetic linkage in size inheritance. Amer. Nat., 66, 87–91.
GREEN, E. L. (1954). Genetics of a new hair deficiency, furless, in the house mouse. J. Hered., 45, 115–118.
GREEN, E. L. (1966). The Jackson laboratory: a center for mammalian genetics in the United States. J. Hered., 57, 2–12.
GREEN, E. L. (1967). Shambling, a neurological mutant of the mouse. J. Hered., 58, 65–68.
GREEN, E. L. (1968). Linkage of shambling with rex in linkage group VII of the mouse. J. Hered., 59, 59.
GREEN, E. L. and MANN, S. J. (1961). Opossum, a semi-dominant lethal mutation affecting hair and other characteristics of mice. J. Hered., 52, 223–227.
GREEN, M. C. (1955). Luxoid, a new hereditary leg and foot abnormality in the house mouse. J. Hered., 46, 90–99.
GREEN, M. C. (1961). The position of luxoid in linkage group II of the mouse. J. Hered., 52, 297–300.
GREEN, M. C. (1963). Methods for testing linkage. In Burdette, W. J. (Editor), Methodology in Mammalian genetics. San Francisco: Holden-Day.
GREEN, M. C. (1966). Mutant genes and linkages. In Green, E. L. (Editor), Biology of the laboratory mouse. New York: McGraw-Hill
GREEN, M. C. (1968). Linkage map of the mouse. In Sober, H. A. (Editor), Handbook of Chemistry. Cleveland: Chemical Rubber Co.
GREEN, M. C. and DICKIE, M. M. (1959). Linkage map of the mouse. J. Hered., 50, 2–5.
GREEN, M. C. and LANE, P. W. (1967). Linkage group II of the house mouse. J. Hered., 58, 225–228.
GREEN, M. C. and SIDMAN, R. L. (1962). Tottering, a neuromuscular mutation in the mouse and its linkage with oligosyndactylism. J. Hered., 53, 233–237.
GREEN, M. C., SNELL, G. D. and LANE, P. W. (1963). Linkage group XVIII of the mouse. J. Hered., 54, 245–247.
GRIFFEN, A. B. (1955). A late pachytene chromosome map of the male mouse. J. Morph., 96, 123–136.
GRIFFEN, A. B. (1958a). Occurrence of chromosomal aberrations in presperematocytic cells of irradiated male mice. Proc. Nat. Acad. Sci. U.S.A., 44, 691–649.
GRIFFEN, A. B. (1958b). Mammalian cytogenetics and the cancer problem. Annals N.Y. Acad. Sci., 71, 1156–1162.
GRIFFEN, A. B. (1960). Mammalian pachytene chromosome mapping and somatic chromosome identification. J. Cell. Comp. Physiol., 56, (Suppl. 1), 113–121.
GRITFEN, A. B. (1966). Nuclear cytology. In Green, E. L. (Editor), Biology of the laboratory mouse. New York: McGraw-Hill.
GRIFFEN, A. B. (1967). A case of tertiary trisomy in the mouse, and its implications for the cytological classification of trisomics in other mammals. Canad. J. Genet. Cytol., 9, 503–510.
GRIFFEN, A. B. and BUNKER, M. C. (1964). Three cases of trisomy in the mouse. Proc. Nat. Acad. Sci. U.S.A., 52, 1194–1198.
GRIFFEN, A. B. and BUNKER, M. C. (1967). Four further cases of autosomal primary trisomy in the mouse. Proc. Nat. Acad. Sci. U.S.A., 58, 1446–1452.
GRUNEBERG, H. (1935). A three factor linkage experiment in the house mouse. J. Genet., 31, 157–172.
GRUNEBERG, H. (1936a). Some linkage tests with wavy mice. J. Genet., 32, 1–3.
GRUNEBERG, H. (1936b). Further linkage data on the albino chromosome of the house mouse. J. Genet., 33, 255–265.
GRUNEBERG, H. (1936c). Inheritance of tail tip pigmentation in the house mouse. J. Genet., 33, 343–345.
GRUNEBERG, H. (1943). Two new mutant genes in the house mouse. J. Genet., 45, 22–28.
GRUNEBERG, H. (1952). The genetics of the mouse. The Hague: Nijhoff.
GRUNEBERG, H. (1956). An annotated catalogue of the mutant genes of the house mouse. Med. Res. Council Mem., 33: 28 pp.
GRUNEBERG, H., BURNETT, J. B. and SNELL, G. D. (1941). The origin of jerker, a new gene mutation of the house mouse and linkage studies made with it. Proc. Nat. Acad. Sci. U.S.A., 27, 562–565.
GRUNEBERG, H. and TRUSLOVE, G. M. (1960). Two closely linked genes in the mouse. Genet., Res., 1, 69–90.
HAGEDOORN, A. L. (1914). Repulsion in mice (a reply). Amer. Nat., 48, 699–700.
HALDANE, J. B. S. (1919). The combination of linkage values and the calculation of distance between the loci of linked factors. J. Genet., 8, 299–309.
HALDANE, J. B. S., SPRUNT, A. D. and HALDANE, N. M. (1915). Reduplication in mice. J. Genet., 5, 133–135.
HAUSCHKA, T. S. (1955). Probable Y linkage of a histocompatibility gene. Transpl. Bull., 2, 154–155.
HAUSCHKA, T. S., GOODWIN, M. B. and BROWN, E. (1951). Evidence for a sex-linked lethal in the house mouse. Genetics, 36, 235–253.
HAUSCHKA, T. S., GRINNELL, S. T., MEAGHER, M. and AMOS, D. B. (1961). Sex-linked incompatibility of male skin and primary tumours transplanted to isologous female mice. XIII Annual Symp. Fundamental Cancer Res., (1959), 271–294.
HAUSCHKA, T. S. and HOLDRIDGE, B. A. (1962). A cytogenetic approach to the Y-linked histocompatibility antigen of mice. Ann. N.Y. Acad. Sci., 101, 12–22.
HAUSCHKA, T. S., JACOBS, B. B. and HOLDRIDGE, B. A. (1968). Recessive yellow and its interaction with belted in the mouse. J. Hered., 59, 339–341.
HAUSCHKA, T. S., MEAGHER, M. A. and HOLDRIDGE, B. A. (1962). Autosomal translocation of the `male antigen’ of mice and immunoselection against the Y chromosome. Inter. Symp. Tissue Transplantation Santiago, 1961, 25–36.
HENDERSON, S. A. and EDWARDS, R. G. (1968). Chiasma frequency and material age in mammals. Nature, 218, 22–28.
HERTWIG, P. (1940). Vererbbare Semisteritat bei Mausen nach Rontgenbestrahlung verursacht durch reziproke chromosomentranslokationen. Z. Ind. Abst. Vererbgslehre 79, 1–29.
HERTWIG, P. (1942). Neue mutationen und Koppelungsgruppen bei der Hausmaus. Z. Ind. Abst. Vererbgslehre, 80, 220–246.
HERZENBERG, L.A. (1964). A chromosome region for gamma 2a and beta 2a globulin H chaim isoantigens in the mouse. Cold Spring Harbor Symp. Quant. Biol., 29, 455–462.
HERZENBERG, L. A., McDEVITT, H. O. and HERZENBERG, L. A. (1968). Genetics of antibodies. Ann. Rev. Genet., 2, 209–244.
HERZENBERG, L. A., MINNA, J. D. and HERZENBERG, L. A. (1967). The chromosome region for immunoglobulin heavy chains in the mouse. Cold Spring Harbor Symp. Quant. BioL, 32, 181–186.
HERZENBERG, L. A., WARNER, N. J. and HERZENBERG, L. A. (1965). Immunoglobulin isoantigens (allotypes) in the mouse. I. Genetics and cross reactions of the 7S 72A-isoantigen controlled by alleles at the IG.1 Locus./ Exp. Med., 121, 415–438.
HESTON, W. E. (1941). Relationship between susceptibility to induced pulmonary tumors and certain known genes in mice. J. Nat. Cancer Inst., 2, 127–132.
HESTON, W. E. (1951). The vestigial tail mouse. J. Hered., 42, 71–74.
HESTON, W. E. (1953). Linkage between pulmonary tumours and vestigial tail in the house mouse. Nature, 172, 1007–1008.
HESTON, W. E., DERINGER, M. K., HUGHES, I. R. and CORNFIELD, J. (1952). Interrelation of specific genes, body weight and development of tumors in mice. J. Nat. Cancer Inst., 12, 1141–1157.
HIRST, B. B. (1957). The influence of sex on transplantability of isologous thymic tissue in normal C57BL mice. Transpl. Bull., 4, 58.
HOECKER, G. (1956). Genetic mechanisms in tissue transplantation in the mouse. Cold Spring Harbor Symp. Quant. Biol., 21, 355–361.
HOECKER, G., MARTINEZ, A., MARKOVIC, S. and PIZARRO, O. (1954). Agitans, a mutation with neurological effects in the house mouse. J. Hered., 45, 10–14.
HOECKER, G. and PIZARRO, O. (1962). The histocompatibility antigens. Inter. Symp. Tissue transplantation Santiago, 1961, 54–71.
HOLLANDER, W. F. and GOWEN, J. W. (1959). A single gene antagonism between mother and foetus in the mouse. Proc. Soc. Exp. Biol. Med., 101, 425–428.
HOLLANDER, W. F., GOWEN, J. W. and STADLER, J. (1956). A study of 25 gynandromorphic mice of the Bagg albino strain. Anat. Rec., 124, 223–244.
HOLLANDER, W. F. and STRONG, L. C. (1951). Pintail, a dominant mutation linked with brown in the house mouse. J. Hered., 42, 179–182.
HUDSON, D. M., FINLAYSON, J. S. and POTTER, M. (1967). Linkage of one component of the major urinary protein complex of mice to the brown coat colour locus. Genet. Res., 10, 195–198.
HUNGERFORD, D. (1955). Chromosome number of 10-day foetal mouse cells. J. Morph., 97, 497.
HUNT, H. R., MIXTER, R. and PERMER, D. (1933). Flexed tail in the mouse. Genetics, 18, 335–366.
HUSKINS, C. L. and HEARNE, E. M. (1934). Chromosome differences in mice susceptible and resistant to cancer. Nature, 133; 615.
HUSKINS, C. L. and HEARNE, E. M. (1936). Spermatocyte chiasma frequency in strains of mice differing in susceptibility or resistance to the spontaneous occurrence of malignant tumours. Canad. J. Res. D., 14, 39–58.
HUTTON, J. J. (1969a). Linkage analysis using biochemical variants in mice. Genetics, 61, s28.
HUTTON, J. J. (1969b). Linkage analyses using biochemical variants in mice. I. Linkage of the hemoglobin beta-chain and glucosephosphate isomerase loci. Biochem. Genet., 3, 507–515.
HUTTON, J. J., BISHOP, J., SCHWEET, R. and RUSSELL, E. S. (1962). Hemoglobin inheritance in inbred mouse strains. II. genetic studies. Proc. Nat. Acad. Sci. U.S.A., 48, 1718–1724.
HUTTON, J. J. and COLEMAN, D. L. (1969). Linkage analyses using biochemical variants in mice. II. Levulinate dehydratase and autosomal glucose 6-phosphate dehydrogenase. Biochem. Genet., 3, 517–523.
HUTTON, J. J. and RODERICK, T. H. (1970). Linkage analyses using biochemical variants in mice. III Linkage relationships of eleven biochemical markers. Biochem. Genet., 4, 339–350.
HUTTON, J. J., SCHWEET, R. S., WOLFE, H. G. and RUSSELL, E. S. (1964). Hemoglobin solubility and x-chain structure in crosses between two inbred. mouse strains. Science, 143, 252–253.
JAFFE, J. (1952). Cytological observations concerning inversion and translocation in the house mouse. Amer. Nat., 86, 101–107.
JOHNSON, D. R. (1969a). Brachyphalangy, an allele of extra-toes in the mouse. Genet. Res., 13, 275–280.
JOHNSON, D. R. (1969b). Polysyndactyly, a new mutant gene in the mouse. J. Embryo!. Exp. Morph., 21, 285–294.
KEELER, C. E. (1927). Rodless retina, an ophthalmic mutation in the house mouse. J. Exp. Zoo, 46, 355–407.
KEELER, C. E. (1930). Hereditary blindness in the house mouse with special reference to the linkage relationship. Harvard Med. School, Howe Lab. Ophthalmol. Bull., 3, 11 pp.
KEELER, C. E. (1931a). The independence of dominant spotting and recessive spotting (piebald) in the house mouse. Proc. Nat. Acad. Sci. U.S.A., 17, 101–102.
KEELER, C. E. (1931b). A probable new mutation to white belly in the house mouse. Proc. Nat. Acad. Sci. U.S.A., 17, 700–703.
KEELER, C. E. (1966). Retinal degeneration in the mouse is rodless retina. J. Hered., 57, 47–50.
KELTON, D. E. and RAUCH, H. (1968). Linkage of open eyelids with linkage group VII of the mouse. J. Hered., 59, 27–28.
KIDWELL, J. F., GOWEN, J. W. and STADLER, J. (1961). Pugnose, a recessive mutation in linkage group III of mice. J. Hered., 52, 145–148.
KIDWELL, J. F., GOWEN, J. W. and STADLER, J. (1966). Pugnose linkage in the mouse. J. Hered., 57, 229–230.
KIDWELL, J. H., NASH, G. D., STADLER, J. and GOWEN, J. W. (1961). An X-ray induced deficiency in linkage group VI of the mouse. Amer. Zool., 1, 365.
KINDRED, B. M. (1961). Abnormal inheritance of the sex-linked Tabby gene. Aust. J. Biol. Sci., 14, 415–418.
KING, J. W. B. (1956). Linkage group XIV of the house mouse. Nature, 178, 1126–1127.
KLEIN, E. and LINDER, O. (1961). Factorial analysis of the reactivity of C57BL females against isologous male skin grafts. Transplantation, 27, 457–459.
KLEIN, J., BEDNAROVA, D. and SCHREFFLER, D. C. (1969). Analysis of the mouse in two translocations stocks and an H-2 crossover. Genetics, 61, s33.
KLEIN, J. and MARTINKOVA, J. (1968). A new non-H-2 antigen of C57BL mice. Folia Biol. (Praha), 14, 237–238.
KOLLER, P. C. (1944). Segmental interchange in mice. Genetics, 29, 247–263.
KOLLER, P. C., and AUERBACH, C. (1941). Chromosome breakage and sterility in the mouse. Nature, 148, 501.
KOLLER, P. C. and DARLINGTON, C. D. (1934). The genetical and mechanical properties of the sex chromosomes. I. Rattus norvegicus. J. Genet., 29, 359–383.
KOSAMBI, D. D. (1944). The estimation of map distances from recombination values. Ann. Eugen., 12, 172–175.
KREITNER, P. C. (1957). Linkage studies in a black-eyed white mutation in the house mouse. J. Hered., 48, 300–304.
KROON, P. H. W. VAN DER and BUIS, A. J. M. (1970). Linkage of dwarf with obese in the mouse. Genetica, 41, 57–60.
KRZANOWSKA, H. (1966). Inheritance of reduced male fertility, connected with abnormal spermatozoa, in mice. Acta Biol. Cracov., Zool. Ser., 9, 61–70.
KRZANOWSKA, H. (1969). Factor responsible for spermatozoan abnormality located on the chromosome in mice. Genet. Res., 13, 17–24.
LAGNEAU, L. E. and MEWISSEN, D. J. (1964). Le caryotype de la souris C57BL/6. C.R. Soc. Biol., 158, 1960–1963.
LANE, P. W. (1963). Whirler mice, a recessive behavior mutation in linkage group VIII. J. Hered., 54, 263–266.
LANE, P. W. (1967). Linkage groups III and XVII in the mouse and the position of the light-ear locus. J. Hered., 58, 21–24.
LANE, L. W. and DICKIE, M. M. (1961). Linkage of wabbler-lethal and hairless in the mouse. J. Hered., 52, 159–160.
LANE, P. W. and DICKIE, M. M. (1968). Three recessive mutations producing disproportionate dwarfing in mice: achondroplasia brachymorphic and stubby. J. Hered., 59, 300–308.
LANE, P. W. and GREEN, E. L. (1967). Pale ear and light ear in the house mouse. J. Hered., 58, 17–20.
LANE, P. W. and GREEN, M. C. (1960). Mahogany, a recessive color mutation in linkage group V of the mouse. J. Hered., 51, 228–230.
LAW, L. W. (1952). The flexed-tail gene and induced anaemia in mice. J. Nat. Cancer Inst., 12, 1119–1126.
LAW, L. W., MORROW, A. G. and GREENSPAN, E. M. (1952). Inheritance of low liver glucuronidase activity in the mouse. J. Nat. Cancer Inst., 12, 909–919.
LEONARD, A. and DEKUNDT, G. (1965). Le caryotype de la souris BALB/c. C.R. Soc. Biol., 159, 2080–2083.
LEONARD, A. and DEKUNDT, G. (1967a). The value of chromosome examination in animal breeding. Z. Vers. Tierk., 9, 109–114.
LEONARD, A. and DEKUNDT, G. (1967b). A new marker for chromosome studies in the mouse. Nature, 214, 504–505.
LEONARD, A. and DEKUNDT, G. (1969a). Etude cytologique d’une translocation chromosome Y-autosome chez la souris. Experientia, 25, 876–877.
LEONARD, A. and DEKUNDT, G. (1969b). Etude d’une translocation de type Robertsonien chez les souris de race AKR. Acta Zool. Pathol. Antwerp., 48, 43–57.
LEVAN, A. (1956). The significance of polyploidy for the evolution of mouse tumours. Exp. Cell Res., 11, 613–629.
LEVAN, A., HSU, T. C. and STICH, (1962). The idiogram of the mouse. Hereditas, 48, 677–687.
LIEBERMANN, R., DRAY, S. and POTTER, M. (1965). Linkage in control of allotypic specificities on two different yG immunoglobulins. Science, 148, 640–642.
LIEBERMANN, R. and POTTER, M. (1966). Close linkage in genes controlling T A and 7G heavy chain structure in BALB/C mice. J. Mol. Biol., 18, 516–528.
LILLY, F. (1966). The inheritance of susceptibility to the Gross leukemia virus in mice. Genetics, 53, 529–539.
LILLY, F. (1967). The location of histocompatibility-6 in the mouse genome. Transplantation, 5, 83–85.
LITTLE, C. C. (1913). Experimental studies of the inheritance of color in mice. Car. Inst. Wash. Pub., 179, 11–102.
LITTLE, C. C. (1915). The inheritance of black-eyed white spotting in mice. Amer. Nat., 49, 727–740.
LITTLE, C. C. (1916). The occurrence of three recognized coat color mutations in mice. Amer. ATat., 50, 335–349.
LITTLE, C. C. (1917). The relation of yellow coat colour and black eyed white spotting of mice in inheritance. Genetics, 2, 433–445.
LITTLE, C. C. (1920). Note on the occurrence of a probable sex-linked factor in mammals. Amer. Nat., 54, 457–460.
LITTLE, C. C. (1927). Notés on a species cross in mice and on an hypothesis concerning the quantitative potentiality of genes. Science, 66, 542–543.
LITTLE, C. C. and PHILLIPS, J. C. (1913). A cross involving four pairs of Mendelian characters in mice. Amer. Nat., 47, 760–762.
LYON, J. B. (1970). The X chromosome and the enzymes controlling muscle glycogen: phosphorylase kinase. Biochem. Genet., 4, 169–185.
LYON, J. B., PORTER, J. and ROBERTSON, M. (1967). Phosphorylase b kinase inheritance in mice. Science, 155, 1550–1551.
LYON, M. F. (1955). Ataxia, a new recessive mutant of the house mouse. J. Hered., 46, 77–80.
LYON, M. F. (1956). Hereditary hair loss in the tufted mutant of the house mouse. J. Hered., 47, 101–103.
LYON, M. F. (1958). Twirler: a mutant affecting the inner ear of the house mouse. J. Embryo!. Exp. Morph., 6, 105–106.
LYON, M. F. (1959). A new dominant T allele in the house mouse. J. Hered, 50, 140–142.
LYON, M. F. (1960a). A further mutation of the mottled type in the house mouse. J. Hered., 51, 116–121.
LYON, M. F. (1960b). Effect of X-rays on the mutation of t alleles in the mouse. Heredity, 14, 247–252.
LYON, M. F. (1961a). Linkage relations and some pleiotropic effects of the dreher mutant of the house mouse. Genet. Res., 2, 92–95.
LYON, M. F. (1961b). Gene action in the X chromosome of the mouse. Nature, 190, 372–373.
LYON, M. F. (1961c). The nature of t alleles in the mouse. Ann. Hum. Genet., 25, 263.
LYON, M. F. (1962). Sex chromatin and gene action in the mammalian X chromosome. Amer. J. Hum. Genet., 14, 135–148.
LYON, M. F. (1963). Attempts to test the inactive X theory of dosage compensation in mammals. Genet. Res., 4, 93–103.
LYON, M. F. (1966a). Order of loci on the X chromosome of the mouse. Genet. Res., 7, 130–133.
LYON, M. F. (1966b). Lack of evidence that inactivation of the mouse X chromosome is incomplete. Genet. Res., 8, 197–203.
LYON, M. F. (1969). A true hermaphrodite mouse presumed to be an XO/XY mosaic. Cytogenetics, 8, 326–331.
LYON, M. F., BUTLER, J. M. and KEMP, R. (1968). The position of the centromeres in linkage groups II and IX of the mouse. Genet. Res., 11, 193–199.
LYON, M. F. and HAWKES, S. G. (1970). An X linked gene for testicular feminization in the mouse. Nature, 227, 1217–1219.
LYON, M. F. and MEREDITH, R. (1964a). Investigations of the nature of t alleles in the mouse. I. Genetic analysis of a series of mutants derived from a lethal allele. Heredity, 19, 301–312.
LYON, M. F. and MEREDITH, R. (1964b). Investigations of the nature of t alleles in the mouse. II. Genetic analysis of an unusual mutant allele and its derivatives. Heredity, 19, 313–325.
LYON, M. F. and MEREDITH, R. (1966). Autosomal translocations causing male sterility and viable anenploidy in the mouse. Cytogenetics, 5, 335–354.
LYON, M. F. and MEREDITH, R. (1969). Muted, a new mutant affecting coat colour and otoliths of the mouse, and its position in linkage group XIV. Genet. Res., 14, 163–166.
LYON, M. F., MORRIS, T., SEARLE, A. G. and BUTLER, J. (1967). Occurrences and linkage relations of the mutant `extra-toes’ in the mouse. Genet. Res., 9, 383–385.
LYON, M. F. and PHILLIPS, R. J. S. (1959). Crossingover in mice heterozygous for t alleles. Heredity, 13, 23–32.
LYON, M. F., SEARLE, A. G., FORD, C. E. and OHNO, S. (1964). A mouse translocation suppressing sex-linked variegation. Cytogenetics, 3, 306–323.
MACDOWELL, E. C. (1950). Light, a new mouse colour. J. Hered., 41, 35–36.
MacNEIL, M. (1956). A mutation to caracul in the house mouse. Nature, 178, 1242.
MAKINO, S. (1941). Studies on the murine chromosomes. I. Cytological investigations of mice included in the genus Mus. J. Fac. Sci. Hokkaido Univ. Ser. VI, Zool., 7, 305–380.
MALLYON, S. A. (1951). A pronounced sex difference in recombination values in the sixth chromosome of the house mouse. Nature, 168, 118–119.
MATHER, K. and NORTH, S. B. (1940). Umbrous: a case of dominance modification in mice. J. Genet., 40, 229–241.
MATTHEY, R. (1953). Les chromosomes des Muridae. Rev. Suisse Zool., 60, 225–283.
McDEVITT, H. O. (1968). Genetic control of the antibody response. III. Qualitative and quantitative characterization of the antibody response to (T.C.)-A-L in CBA and C57 mice. J. Immunol., 100, 485–492.
McDEVITT, H. O. and TYAN, M. L. (1968). Genetic control of the antibody response in inbred mice. J. Exp. Med., 128, 1–11.
McLAREN, A. (1960). New evidence of imbalanced sex chromosome constitution in the mouse. Genet. Res., 1, 253–261.
McNUTT, W. (1967). Porcine tail, a new mutation in the house mouse. Anat. Rec., 157, 286.
MEDVEDEV, N. N. and EGOROV, I. K. (1966). (A histocompatibility gene located in the Y chromosome of CC57BR and CC57W mice.) Genetika (Mosk.) 1966 (8), 86–88.
MICHIE, D. (1952). A new linkage in the mouse: vestigial and rex. Nature, 170, 585.
MICHIE, D. (1953). Affinity: a new genetic phenomenon in the house mouse. Evidence from distant crosses. Nature, 171, 26–27.
MICHIE, D. (1955a). Genetic studies with vestigial tail mice. I. The sex difference in crossingover between vestigial and rex. J. Genet., 53, 270–279.
MICHIE, D. (1955b). Genetical studies with vestigial tail mice. II. The position of vestigial in the VII linkage group. J. Genet., 53, 280–284.
MICHIE, D. (1955c). Genetical studies with vestigial tail mice. III. New independence data. J. Genet., 53, 285–294.
MICHIE, D. (1955d). Affinity. Proc. Roy. Soc., B, 144, 241–259.
MICHIE, D. and McLAREN, A. (1958). A proposed genetic analysis of the Eichwald-Silmser effect. Transpl. Bull., 5, 17–18.
MINNA, J. D., IVERSON, G. M. and HERZENBERG, L. A. (1967). Identification of a gene locus for 7G1 immunoglobulin H chains and its linkage to the H chain chromosome region in the mouse. Proc. Nat. Acad. Sci. U.S.A., 58, 188–194.
MORGAN, T. H. (1914). Multiple allelomorphs in mice. Amer. Nat., 48, 449458.
MORRIS, T. (1968). The XO and OY chromosome constitutions in the mouse. Genet. Res., 12, 125–137.
MURRAY, J. M. (1933). Leaden, a recent color mutation in the house mouse. Amer. Nat., 67, 278–283.
MURRAY, J. M. and SNELL, G; D. (1945). Belted, a new sixth chromosome mutation in the mouse. J. Hered., 36, 266–268.
NAKAMURA, A. and TONOMURA, A. (1963). A characteristic chromosome found in the karyotype analysis of the mouse. Ann. Rep. Nat. Inst. Genet. Jap., 13, 32–33.
NAKAMURA, A. and TONOMURA, A. (1964). An unusual Y chromosome found in a strain of mice. Rep. Nat. Inst. Genet. Jap., 14, 47–48.
NASH, D. J. and VENIER, L. H. (1964). Genetics of grizzle-belly. Proc. Pa. Acad. Sci., 38, 11.
NASRAT, G. S. (1956). Estimation of the recombination fraction between two linked genes Re and sh-2 in the house mouse. Proc. Zool. Soc. Bengal, 9, 85–87.
OHNO, S. and CATTANACH, B. M. (1962). Cytological study of an X autosome translocation in Mus musculus. Cytogenetics, 1, 129–140.
OHNO, S., CHRISTIAN, C. and STENIUS, C. (1963). Significance in mammalian oogenesis of the non-homologous association of bivalents. Exp. Cell Res., 32, 590–592.
OHNO, S., KAPLAN, W. D. and KINOSITA, R. (1957a). Note on non-chiasma type association between the X and Y chromosomes of Drosophila melanogaster and Mus musculus. Exp. Cell Res., 13, 42 2424.
OHNO, S., KAPLAN, W. D. and KINOSITA, R. (1957b). Heterochromatic regions and nucleolus organizers in chromosomes of the mouse. Exp. Cell Res., 13, 358–364.
OHNO, S., KAPLAN, W. D. and KINOSITA, R. (1959a). On the end-to-end association of the X and Y chromosomes of Mus musculus. Exp. Cell Res., 18, 282–290.
OHNO, S., KAPLAN, W. D. and KINOSITA, R. (1959b). Do XY and O sperm occur in Mus musculus? Exp. Cell res., 18, 382–384.
OHNO, S. and LYON, M. F. (1965). Cytological study of Searle’s X chromosome translocation in Mus musculus. Chromosoma, 16, 90–100.
OJIMA, Y., TAKAYAMA, S. and KATO, F. (1965). A study of the sex chromosomes in the mouse. Japan J. Genet., 40, 319–324.
OMURA, T. (1968). Temporary centric connection of chromosomes in normal mice. Proc. XII Inter. Gongr. Genet. Tokyo, 1, 162.
OWEN, A. R. G. (1949). The theory of genetical recombination. I. Long chromosome arms. Proc. Roy. Soc. B, 136, 67–94.
OWEN, A. R. G. (1950). The theory of genetical recombination. Advanc. Genet., 3, 117–157.
OWEN, A. R. G. (1953a). Super-recombination in the sex chromosome of the mouse. Heredity, 7, 103–110.
OWEN, A. R. G. (1953b). The analysis of multiple linkage data. Heredity, 7, 247–264.
PAIGEN, K. and NOELL, W. K. (1961). Two linked genes showing a similar timing of expression in mice. Nature, 190, 148–150.
PAINTER, T. S. (1927). The chromosome constitution of Gate’s ‘non-disjunction’ mice. Genetics, 12, 379–392.
PAINTER, T. S. (1928a). A comparison of the chromosomes of the rat and mouse. Genetics, 13, 180–189.
PAINTER, T. S. (1928b). The chromosome constitution of the Little and Bagg abnormal eyed mice. Amer. Nat., 62, 284–286.
PARSONS, P. A. (1958a). A balanced four-point linkage experiment for linkage group XIII of the house mouse. Heredity, 12, 77–95.
PARSONS, P. A. (1958b). Additional three-point data for linkage group V of the mouse. Heredity, 12, 357–362.
PARSONS, P. A. (1958c). On the phenomenon of genetic interference. Proc. X Inter. Congr. Genet., 2, 213.
PARSONS, P. A. (1959). Possible affinity between linkage groups V and XIII of the house mouse. Genetica, 29, 304–311.
PASSMORE, H. C. and SHREFFLER, D. C. (1968). A sex-limited serum protein variant associated with the H-2 region of the mouse. Genetics, 60, 210–211.
PASSMORE, H. C. and SHREFFLER, D. C. (1970). A sex-limited serum protein variant in the mouse: inheritance and association in the H-2 region. Biochem. Genet., 4, 351–365.
PEARSON, P. L. and Bobrow, M. (1970). Definitive evidence for the short arm of the Y chromosome associating with the X chromosome during meiosis in the human male. Nature, 226, 959–961.
PELT, A. F. VAN, CAIN, K. and KNORR, R. (1969). A new hairless mutant in the house mouse. J. Hered., 60, 75, 96.
PELZER, C. F. (1965). Genetic control of erythrocyte esterase forms in Mus musculus. Genetics, 52, 819–828.
PETRAS, M. L. and BIDDLE, F. G. (1967). Serum esterases in the house mouse. Canad. J. Genet. CytoL, 9, 704–710.
PETRAS, M. L. and SINCLAIR, P. (1969). Another esterase variant in the kidney of the house mouse. Canad. J. Genet. CytoL, 11, 97–102.
PHILLIPS, R. J. S. (1954). Jimpy, a new totally sex-linked gene in the house mouse. Z. Ind. Abst. Vererbgslehre., 86, 322–326.
PHILLIPS, R. J. S. (1956). The linkages of congenital hydrocephalus in the house mouse. J. Hered., 47, 302–304.
PHILLIPS, R. J. S. (1960). Lurcher, a new gene in linkage group XI of the house mouse. J. Genet., 57, 35–42.
PHILLIPS, R. J. S. (1961). Dappled, a new allele at the mottled locus in the house mouse. Genet. Res., 2, 290–295.
PHILLIPS, R. J. S. (1963). Striated, a new sex-linked gene in the house mouse. Genet. Res., 4, 151–153.
PHILLIPS, R. J. S. (1966). A cis-trans position effect at the A locus of the house mouse. Genetics, 54, 485–495.
PIERRO, L. J. and CHASE, H. B. (1963). Slate, a new coat colour mutant in the mouse. J. Hered., 54, 46–50.
PINCUS, G. (1929). A spontaneous mutation in the house mouse. Proc. Nat. Acad. Sci. U.S.A., 15, 85–88.
PIZARRO, O. and DUNN, L. C. (1970). A study of recombination between the H-2 locus and loci closely linked with it in the house mouse. Transplantation, 9, 207–218.
PIZARRO, O., HOECKER, G., RUBINSTEIN, P. and RAMOS, A. (1961). The distribution in the tissues and the development of H-2 antigens of the mouse. Proc. Nat. Acad. Sci. U.S.A., 47, 1900–1907.
PLATE, L. (1910). Die Erbformeln der Farbenrassen von Mus musculus. ZooL Anz., 35, 634–640.
PLATZ, R. D. and WOLFE, H. G. (1969). Mouse seminal vesicle proteins. J. Hered., 60, 187–192.
POPP, D. M. (1967a). A description of rho: a non-H-2 isoantigen in RFM mice. Transplantation, 5, 290–299.
POPP, D. M. (1967b). A review of non-H-2 isoantigens in mice. Transplantation, 5, 300–309.
POPP, D. M. (1969). Histocompatibility–14: correlation of the isoantigen rho and the R–Z locus. Transplantation, 7, 233–241.
POPP, R. A. (1962a). Studies on the mouse hemoglobin loci. H. Position of the hemoglobin locus with respect to albinism and shaker-1 loci. J. Hered., 53, 73–75.
POPP, R. A. (1962b). Studies on the mouse hemoglobin loci. III. Heterogeneity of electrophoretically indistinguishable single type hemoglobin. J. Hered., 53, 75–77.
POPP, R. A. (1962c). Studies on the mouse hemoglobin loci. IV. Independent segretation of Hb and SOL. J. Hered., 53, 77–80.
POPP, R. A. 1962d ). Studies on the mouse hemoglobin loci. VI. A third allele, SOL, at the SOL locus. J. Hered., 53, 147–148.
POPP, R. A. (1965). Loci linkage of serum esterase patterns and oligosyndactylism. J. Hered., 56, 107–108.
POPP, R. A. (1967). Linkage of Es-1 and Es-2 in the mouse. J. Hered., 58, 186–188.
POPP, R. A. (1969a). Studies on the mouse hemoglobin loci. VIII. A fourth a-chain phenotype. J. Hered., 60, 126–128.
POPP, R. A. (1969b). Studies on the mouse hemoglobin loci. IX. A fifth a-chain phenotype. J. Hered., 60, 128–131.
POPP, R. A. (1969c). Studies on the mouse hemoglobin loci. X. Linkage of duplicate genes at the a-chain locus Hba. J. Hered., 60, 131–133.
POPP, R. A. and AMAND, W. S. (1960). Studies on the mouse hemoglobin locus. I. Identification of hemoglobin types and linkage of hemoglobin with albinism. J. Hered., 51, 141–144.
POPP, R. A. and AMAND, W. S. (1964). A sex difference in recombination frequency in the albinism-hemoglobin interval of linkage group I in the mouse. J. Hered., 55, 101–103.
POPP, R. A. and HILSE, K. (1968). Alpha chains of hemoglobins among laboratory mice. Genetics, 60, 212.
POTTER, M. and LIEBERMAN, R. (1967). Genetics of immunoglobulins in the mouse. Advanc. Immunol., 7, 92–145.
PREHN, R. T. and MAIN, J. M. (1956). The influence of sex on isologous skin grafting in the mouse. J. Nat. Cancer Inst., 17, 35–36.
REED, S. C. (1937). The inheritance and expression of fused, a new mutation in the house mouse. Genetics, 22, 1–13.
REID, D. H. and PARSONS, P. A. (1963). Sex of parent and variation of recombination with age in the mouse. Heredity, 18, 107–108.
ROBERTS, E. and QUISENBERG, J. H. (1935). Linkage of the genes for non-yellow and pink-eyed-2 in the house mouse. Amer. Nat., 69, 181–183.
ROBERTS, R. C. (1967). Small eyes, a new dominant eye mutant in the mouse. Genet. Res., 9, 121–122.
ROBINS, M. W. (1959). A mutation causing congenital clubfoot in the house mouse. J. Hered., 50, 188–192.
ROBINSON, R. (1959). Sable and umbrous mice. Genetica, 29, 319–326.
RODERICK, T. H., HUTTON, J. J. and RUDDLE, F. H. (1970). Linkage of esterase-3 (Es-3) and rex (Re) in linkage group VII of the mouse. J. Hered., 61, 278–279.
RUDDLE, F. H. and RODERICK, T. H. (1965a). The genetic control of three kidney esterases in C57BL/6J and RF/J mice. Genetics, 51, 445–454.
RUDDLE, F. H. and RODERICK, T. H. (1965b). Allelically determined isozyme polymorphisms in laboratory populations of mice. Annals N.Y. Acad. Sci., 151, 531–539.
RUDDLE, F. H. and RODERICK, T. H. (1966). The genetic control of two types of esterases in inbred strains of the mouse. Genetics, 54, 191–202.
RUDDLE, F. H., SHOWS, T. B. and RODERICK, T. H. (1968). Autosomal control of an electrophoretic variant of glucose-6-phosphate dehydrogenase in the mouse. Genetics, 58, 599–606.
RUDDLE, F. H., SHOWS, T. B. and RODERICK, T. H. (1969). Esterase genetics in Mus musculus: expression, linkage and polyporphism of locus Es-2. Genetics, 62, 393–399.
RUNNER, M. N. (1959). Linkage of brachypodism. J. Hered., 50, 81–84.
RUSSELL, E. S. and McFARLAND, E. C. (1966). Analysis of pleiotropic effects of W and f genic substitutions in the mouse. Genetics, 53, 949–959.
RUSSELL, E. S., NASH, D. J., BERNSTEIN, S. E., KENT, E. L., MACFARLAND, E. C., MATTHEWS, S. M. and NORWOOD, M. S. (1970) Characterization and genetic studies of microcytic anemia in house mouse. Blood, 35, 838–850.
RUSSELL, L. B. (1961). Genetics of mammalian sex chromosomes. Science, 133, 1795–1803.
RUSSELL, L. B. (1962). Chromosome aberrations in experimental mammals. Progress Med. Genetics, 2, 230–294.
RUSSELL, L. B. (1963). Mammalian X chromosome action: inactivation limited in spread and in region of origin. Science, 31, 976–978.
RUSSELL, L. B. (1967). Complementation mapping of a small region of linkage group II in the mouse. Genetics, 56, 585.
RUSSELL, L. B. and BANGHAM, J. W. (1961). Variegated type position effects in the mouse. Genetics, 46, 509–525.
RUSSELL, L. B., BANGHAM, J. W. and SAYLORS, C. L. (1962). Delimitation of chromosomal regions involved in V-type position effects from X-autosome translocations in the mouse. Genetics, 47, 981–982.
RUSSELL, L. B. and CHU, E. H. Y. (1961). An XXY male in the mouse. Proc. Nat. Acad. Sci. U.S.A., 47, 571–575.
RUSSELL, L. B., McDANIEL, M. N. C. and WOODIEL, F. N. (1963). Crossingover within the a locus of the mouse. Genetics, 48, 907.
RUSSELL, L. B. and MONTGOMERY, C. S. (1965). The use of X-autosome translocations in locating the X chromosome inactivation center. Genetics, 52, 470–471.
RUSSELL, L. B. and MONTGOMERY, C. S. (1969). Comparative studies on X-autosome translocations in the mouse. I. Origin viability, fertility and weight of five (X,1)’s. Genetics, 63, 103–120.
RUSSELL, L. B. and MONTGOMERY, C. S. (1970). Comparative studies on X-autosome translocations in the mouse. II. Inactivation of autosomal loci, segregation and mapping of autosomal breakpoints in five T(X;1)’s. Genetics, 64, 281–312.
RUSSELL, L. B. and RUSSELL, W. L. (1960). Genetic analysis of induced deletions and of spontaneous nondisjunction involving chromosome 2 of the mouse. J. Cell. Comp. PhysioL, 56 (Suppl. 1), 169–188.
RUSSELL, L. B. and SAYLORS, C. L. (1962). Induction of parternal sex chromosome losses by irradiation of mouse spermatozoa. Genetics, 47, 7–10.
RUSSELL, L. B., STEELE, M. S. and THOMPSON, H. M. (1966). Deficiencies in the mouse. U.S. Atom. Energy Corn. Rep., ORNL, 3999, 90–92.
RUSSELL, W. L., RUSSELL, L. B. and GOWER, J. S. (1959). Exceptional inheritance of a sex-linked gene in the mouse explained on the basis that the XO sex chromosome constitution is female. Proc. Nat. Acad. Sci. U.S.A., 45, 554–560.
SACHS, L. (1955). The possibilities of crossingover between the sex chromosomes of the house mouse. Genetica, 27, 309–322.
SACHS, L, and HELLER, E. (1958). The sex-linked histocompatibility antigens. J. Nat. Cancer Inst., 20, 555–561.
SARVELLA, P. A. and RUSSELL, L. B. (1956). Steel, a new dominant gene in the house mouse with effects on coat pigment and blood. J. Hered, 47, 123–218.
SCHAIBLE, R. and GOWEN, J. W. (1961). A new dwarf mouse. Genetics, 46, 896.
SCHLESINGER, K., ELSTON, R. C. and BOGGAN, W. (1966). The genetics of sound induced seizure in inbred mice. Genetics, 54, 95–103.
SEARLE, A. G. (1961). Tipsy, a new mutant in linkage group VII of the mouse. Genet. Res., 2, 122–216.
SEARLE, A. G. (1964). The genetics and morphology of two luxoid mutants in the house mouse. Genet. Res., 5, 171–197.
SEARLE, A. G. (1966). Curtailed, a new dominant T-allele in the house mouse. Genet. Res., 7, 86–95.
SEARLE, A. G., BERRY, R. J. and BEECHEY, C. V. (1970). Cytogenetic radio-sensitivity and chiasma frequency in wild living male mice. Mutation Res., 9, 137–140.
SEARLE, A. G. and TRUSLOVE, G. M. (1970). A gene triplet in the mouse. Genet. Res., 15, 227–235.
SHORT, B. F. and SOBEY, W. R. (1957). The effect of sex on skin grafts within inbred lines of mice. Transpl. Bull., 4, 110–112.
SHOWS, T. B. and RUDDLE, F. H. (1968). Function of the lactate dehydrogenase B gene in mouse erythrocytes: evidence for control by a regulatory gene. Proc. Nat. Acad. Sci. U.S.A., 61, 574–581.
SHOWS, T. B., RUDDLE, F. H. and RODERICK, T. H. (1969). Phosphoglucomutase electrophoretic variants in the mouse. Biochem. Genet., 3, 25–35.
SHREFFLER, D. C. (1960), Genetic control of serum transferrion type in mice. Proc. Nat. Acad. Sci. U.S.A., 46, 1378–1384.
SHREFFLER, D. C. (1963). Linkage of the mouse transferrion locus. J. Hered., 54, 127–129.
SHREFFLER, D. C. (1964a). Inheritance of a serum pre-albumin variant in the mouse. Genetics, 49, 629–634.
SHREFFLER, D. C. (1964b). A seriologically detected variant in mouse serum: further evidence for genetic control by the histocompatibility-2 locus. Genetics, 49, 973–978.
SHREFFLER, D. C. (1964c). A further subdivision of the complex H-2 region of the mouse. Genetics, 50, 285.
SHREFFLER, D. C. (1965). The Ss system of the mouse. Wistar Inst. Symp. Monogr., 3, 11–19.
SHREFFLER, D. C. (1966). A new erythrocytic antigen in the house mouse. Genetics, 54, 362.
SHREFFLER, D. C. (1967). Genetic control of cellular antigens. Proc. III Inter. Congr. Human Genet., 217–231.
SHREFFLER, D. C., AMOS, D. B. and MARK, R. (1966). Serological analysis of a recombination in the H-2 region of the mouse. Transplantations, 4, 300–322.
SHREFFLER, D. C. and OWEN, R. D. (1963). A serologically detected variant in mouse serum: inheritance and association with the histocompatibility-2 locus. Genetics, 48, 9–25.
SHREFFLER, D. C. and SNELL, G. D. (1969). The distribution of thirteen H-2 allo-antigenic specificities among the products of eighteen H-2 alleles. Transplantation, 8, 435–450.
SICK, K. and NIELSEN,,J. T. (1964). Genetics of amylase isozymes in the mouse. Hereditas, 51, 291–296.
SIDMAN, R. L. and GREEN, M. C. (1965). Retinal degeneration in the mouse. Location of the rd locus in linkage group XVII. J. Hered., 56, 23–29.
SIDMAN, R. L., GREEN, M. C. and APPEL, S. H. (1965). Catalog of the neurological mutants of the mouse. Cambridge, Mass.: Harvard University Press.
SIDMAN, R. L., LANE, P. W. and DICKIE, M. M. (1962). Staggerer, a new mutation in the mouse affecting the cerebellum. Science, 137, 610–612.
SILAGI, S. (1962). A genetical and embryological study of partial complementation between lethal alleles at the T locus of the house mouse. Devel. Biol., 5, 35–67.
SILVERS, W. K. and BILLINGHAM, R. E. (1967). Genetic background and expressivity of histocompatibility genes. Science, 158, 118–119.
SILVERS, W. K., BILLINGHAM, R. E. and SANFORD, B. H. (1968). The H-Y transplantation antigen: a Y linked or sex influenced factor? Nature, 220, 401–403.
SIRLIN, J. L. (1956). Vacillans, a neurological mutant in the house mouse linked with brown. J. Genet., 54, 42–48.
SIRLIN, J. L. (1957). Location of vacillans in linkage group VIII of the house mouse. Heredity, 11, 259–260.
SLIZYNSKI, B. M. (1949). A preliminary pachytene chromosome map of the house mouse. J. Genet., 49, 242–245.
SLIZYNSKI, B. M. (1952). Pachytene analysis of Snell’s T(5:8)a translocation in the mouse. J. Genet., 50, 507–510.
SLIZYNSKI, B. M. (1954). Partial sex-linkage in the mouse. Nature, 174, 310.
SLIZYNSKI, B. M. (1955a). Chiasmata in the male mouse. J. Genet., 53, 597–605.
SLIZYNSKI, B. M. (1955b). The sex bivalent of Mus musculus. J. Genet., 53, 591–596.
SLIZYNSKI, B. M. (1957b). Chromosomal mechanism in translocation infertility. Proc. Roy. Phys. Soc. Edin., 26, 49–60.
SLIZYNSKI, B. M. (1957a). Cytological analysis of translocations in the mouse. J. Genet., 55, 122–130.
SLIZYNSKI, B. M. (1958). Chiasmata in female mice. Proc. X Inter. Congr. Genet., 2, 264.
SLIZYNSKI, B. M. (1960). Sexual dimorphism in mouse gametogenesis. Genet. Res., 1, 477–486.
SLIZYNSKI, B. M. (1964). Cytology of the XXY mouse. Genet. Res., 5, 328–329.
SLIZYNSKI, B. M. (1967). Oocyte pachytene analysis of Cattanach’s fd translocation. Genet. Res., 9, 17–22.
SNELL, G. D. (1928). A crossover between the genes for short-ear and density in the house mouse. Proc. Nat. Acad. Sci. U.S.A., 14, 926–928.
SNELL, G. D. (1931). Inheritance in the house mouse; the linkage relations of short-ear, hairless and naked. Genetics, 16, 42–74.
SNELL, G. D. (1933). Genetic changes in mice induced by X-rays. Amer. Nat., 67, 24–31.
SNELL, G. C. (1935). The induction by X-rays of hereditary changes in mice. Genetics, 20, 545–567.
SNELL, G. D. (1941). Gene and chromosome mutations. In Snell, G. D., (Editor). Biology of the laboratory mouse. New York: McGraw-Hill Book Co.
SNELL, G. D. (1945). Linkage of jittery and waltzing in the mouse. J. Hered., 36, 279–280.
SNELL, G. D. (1946). An analysis of translocations in the mouse. Genetics, 31, 157–180.
SNELL, G. D. (1952). Preliminary data on crossingover between H-2 and Fu, Ki and T in the house mouse. Heredity, 6, 247–254.
SNELL, G. D. (1955). Ducky, a new second chromosome mutation in the mouse. J. Hered., 46, 27–29.
SNELL, G. D. (1956). A comment on Eichwald and Silmer’s communication. Transpl. Bull., 3, 29–31.
SNELL, G. D. (1958). Histocompatibility genes of the mouse. II. Production and analysis of isogenic resitant lines. J. Nat. Cancer Inst., 21, 843–877.
SNELL, G. D. and AMES, F. B. (1939). Hereditary changes in the descendants of female mice exposed to Roentgen rays. Amer. J. Roent. Rad. Therap., 41, 248–255.
SNELL, G. D., BODEMANN, E. and HOLLANDER, W. (1934). A translocation in the house mouse and its effects on development. J. Exp. ZooL, 67, 93–104.
SNELL, G. D. and BORGES, P. R. F. (1953). Determination of the histocompatibility locus involved in the resistance of mice of strains C57BL/10-x, C57BL/6-x and C57BL/6Ks to C57BL tumors. J. Nat. Cancer Inst., 14, 481–484.
SNELL, G. D. and BUNKER, H. P. (1964). Histocompatibility genes of mice. IV. The position of H-3 in the fifth linkage group. Transplantation, 2, 743–751.
SNELL, G. D., GUDKOWICZ, G. and BUNKER, H. P. (1967). Histocompatibility genes of mice. VIII. H-13, a new histocompatibility locus in the fifth linkage group. Transplantation, 5, 492–503.
SNELL, G. D., DICKIE, M. M., SMITH, P. and KELTON, D. E. (1954). Linkage of loop-tail, leaden, splotch and fuzzy in the mouse. Heredity, 8, 271–273.
SNELL, G. D. and HIGGINS, G. F. (1951). Alleles at the histocompatibility-2 locus in the mouse as determined by tumor transplantation. Genetics, 36, 306–310.
SNELL, G. D., HOECKER, G., AMOS, D. B. and STIMPFLING, J. H. (1964). A revised nomenclature for the histocompatibility-2 locus of the mouse. Transplantation, 2, 777–784.
SNELL, G. D., HOECKER, G. and STIMPFLING, J. H. (1967). Evidence that the ‘R’ and `Z’ blood group specificities of mice are allelic and distinct from H-2. Transplantation, 5, 481–491.
SNELL, G. D. and LAW, L. W. (1939). Linkage between shaker-2 and wavy-2 in the house mouse. J. Hered., 30, 447.
SNELL, G. D., SMITH, P. and GABRIELSON, F. (1953). Analysis of the histocompatibility-2 locus in the mouse. J. Nat. Cancer Inst., 14, 457–480.
SNELL, G. D. and STEVENS, L. C. (1961). Histocompatibility genes of mice. III. H-1 and H-4, two histocompatibility loci in the first linkage group. Immunology, 4, 366–379.
SOLARI, A. J. (1970). The spatial relationship of the X and Y chromosomes during meiotic prophase in mouse spermatocytes. Chromosoma, 29, 217–238.
SORSBY, A., KOLLER, P. C., ATTFIELD, M., DAVEY, J. B. and LUCAS, D. R. (1954). Retinal dystrophy in the mouse: histological and genetic aspects. J. Exp. ZooL, 125, 171–197.
STEINBERG, A. G. and FRASER, F. C. (1943). Marcelled, a new recessive mutation affecting the coat of the house mouse. Genetics, 28, 92.
STEVENS, L. C. and BUNKER, M. C. (1964). Karyotype and sex of primary testicular teratomes in mice. J. Nat. Cancer Inst., 33, 65–78.
STICH, J. H. and HSU, T. C. (1960). Cytological identification of male and female somatic cells in the mouse. Exp. Cell Res., 20, 248–249.
STIMPFLING, J. H. and RICHARDSON, A. (1965). Recombination within the histocompatibility-2 locus in the mouse. Genetics, 51, 831–846.
STIMPFLING, J. H. and SNELL, G. D. (1968). Detection of a non-H-2 blood group system with the aid of B10.129(5M) mice. Transplantation, 6, 468–475.
STRONG, L. C. (1946). Linkage and crossingover between black pigmentation and susceptibility to induced fibrosarcoma in mice. Science, 103, 554.
TATCHELL, J. A. H. (1961a). Pulmonary tumours, group VII and sex in the house mouse. Nature, 190, 837–838.
TATCHELL, J. A. H. (1961b). Pulmonary tumours and group VII in the house mouse. Nature, 190, 1125.
TSUJI, S. and MEIER, H. (1969). Linkage of serum esterase and tottering in the mouse. J. Hered., 60, 221–222.
TUTIKAWA, K. (1955). Test for allelism of alopecia periodica and furless in the house mouse. Ann. Rep. Nat. Inst. Genet., Japan, 5, 16
WACHTER, W. L. (1921). Data concerning linkage in mice. Amer. Nat., 55, 412–420.
WACHTER, W. L. (1927). Linkage studies in mice. Genetics, 12, 108–114.
WALLACE, M. E. (1950). Locus of the fidget gene in the house mouse. Nature, 166, 407.
WALLACE, M. E. (1953). Affinity: a new genetic phenomenon in the house mouse. Evidence from within laboratory stocks. Nature, 171, 27–28.
WALLACE, M. E. (1954). A mutation or a crossover in the house mouse. Heredity, 8, 89–105.
WALLACE, M. E. (1957a). A balanced three-point experiment for linkage group V of the house mouse. Heredity, 11, 223–258.
WALLACE, M. E. (1957b). The use of affinity in chromosome mapping. Biometrics, 13, 98–110.
WALLACE, M. E. (1958a). New linkage and independence data for ruby and jerker in the mouse. Heredity, 12, 453–462.
WALLACE, M. E. (1958b). Experimental evidence for a new genetic phenomenon. Phil. Trans. Roy. Soc., 241, 211–254.
WALLACE, M. E. (1959). An experimental test of the hypothesis of affinity. Genetica, 29, 243–255.
WALLACE, M. E. (1961). Affinity: evidence from crossing inbred lines of mice. Heredity, 16, 1–23.
WALLACE, M. E. (1965). Pseudoallelism at the agouti locus in the mouse. J. Hered., 56, 267–271.
WALLACE, M. E. and HERBERTSON, B. M. (1969). Neonatal intestinal lipidosis in mice. J. Med. Genet., 6, 361–375.
WATSON, M. L. and OLIVER, J. D. (1965). Chromosomes of the laboratory mouse. Proc. Iowa Acad. Sci, 72, 537–538.
WELSHONS, W. J. and RUSSELL, L. B. (1959). The Y chromosome as the bearer of male determining factors in the mouse. Proc. Nat. Acad. Sci. U.S.A., 45, 560–566.
WHITE, B. J. and TJIO, J. H. (1967). A mouse translocation with 38 and 39 chromosomes but normal N.F. Hereditas, 58, 284–296.
WOLFE, H. G. (1967). Mapping the hemoglobin locus in mice transmitting the flecked translocation. Genetics, 55, 213–218.
WOLFE, H. G., RUSSELL, E. S. and PACKER, S. O. (1963). Hemoglobins in mice. Segregation of genetic factors affecting electrophoretic mobility and solubility. J. Hered., 54, 107–112..
WOOLLEY, G. W. (1945). Misty dilution in the mouse. J. Hered., 36, 269–270.
WORTIS, H. H. (1965). A gene locus concerned with an antigenic serum substance in Mus musculus. Genetics, 52, 267–273.
WRIGHT, M. E. (1947a). Undulated: a new genetic factor in Mus musculus affecting the spine and tail. Heredity, 1, 137–141.
WRIGHT, M. E. (1947b). Two sex-linkages in the house mouse with unusual recombination values. Heredity, 1, 349–354.
YOON, C. H. (1959). Waddler, a new mutation, and its interaction with quivering. J. Hered., 50, 238–244.
YOON, C. H. (1961). Linkage relationship of the waddler gene in mice with evidence for temperature effect in crossingover. J. Hered., 52, 279–281.
YOON, C. H. (1969). Disturbances in developmental pathways leading to a neurological disorder of genetic origin, leaner, in mice. Develop. Biol., 20, 158–181.
YOON, C. H. and LES, E. P. (1957). Quivering, a new first chromosome mutation in mice. J. Hered., 48, 176–180.
YOSIDA, T. H. (1960a). Study on the new mutant ‘falter’ found in the house mouse. Ann. Rep. Nat. Inst. Genet. Japan, 10, 30–31.
YOSIDA, T. H. (1960b). Genetical study on the new mutant ‘falter’ found in the house mouse. Bull. Exp. Anim., 9, 179–182.
ZAALBERG, O. B. (1959). An analysis of the Eichwald-Silmser effect. Transpl. Bull., 6, 433–435.
ZELENY, V. (1967). Morphological identification of the murine Y chromosome. Folia Biol. (Praha), 13, 158–159.
Rights and permissions
Copyright information
© 1972 Springer Science+Business Media New York
About this chapter
Cite this chapter
Robinson, R. (1972). House Mouse. In: Gene Mapping in Laboratory Mammals. Springer, Boston, MA. https://doi.org/10.1007/978-1-4899-7323-8_1
Download citation
DOI: https://doi.org/10.1007/978-1-4899-7323-8_1
Publisher Name: Springer, Boston, MA
Print ISBN: 978-1-4899-7302-3
Online ISBN: 978-1-4899-7323-8
eBook Packages: Springer Book Archive