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New Techniques in the Study of Human Chromosomes: Methods and Applications

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Advances in Human Genetics

Part of the book series: Advances in Human Genetics ((AHUG,volume 5))

Abstract

In 1968, Caspersson et al 10 demonstrated that the fluorescence of chromosomes after quinacrine mustard staining revealed a typical pattern of bands for each element. The importance of this breakthrough was apparently not grasped immediately by cytogeneticists. It was only when Caspersson et al.17,18 demonstrated that each human chromosome could be identified by this technique that banding patterns were studied the world over. A labeling of the pericentromeric regions was achieved by many authors.2,60,82 Very soon other methods derived from these findings were described by Sumner et al.,101 Drets and Shaw,27 and Schnedl.96 Before these developments, the controlled denaturation of chromosomes by heat was described by Dutrillaux and Lejeune,41 using a procedure derived from the experiments of Yunis et al 107 In mid-1971, another technique, proteolytic digestion, was discovered by Dutrillaux et al 36 and numerous modifications were then reported.47,97,105 Finally, modification of the pH of the Giemsa stain solution was described by Patil et al,84 and, in a very different way, Zakharov et al 108 demonstrated that treatment of living cells with 5-bromodeoxyuridine (BUdR) could reveal a specific pattern of localized uncoiling.

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Bibliography

  1. Arrighi, F. E., and Hsu, T. C., Localization of heterochromatin in human chromosomes, Cytogenetics 10: 81 (1971).

    Article  PubMed  CAS  Google Scholar 

  2. Arrighi, F. E., Hsu, T. C., Saunders, P., and Saunders, G. F., Localization of repetitive DNA in the chromosomes of Microtus agrestis by means of in situ hybridization, Chromosoma 32: 224 (1970).

    PubMed  CAS  Google Scholar 

  3. Baranovskaya, L. T., Zakharov, A. F., Dutrillaux, B., Carpentier, S., Prieur, M., and Lejeune, J., Différenciation des chromosomes X par les méthodes de déspirali- sation au 5 bromodéoxyuridine (BUDR) et de dénaturation thermique ménagée, Ann. Genet 15: 271 (1972).

    PubMed  CAS  Google Scholar 

  4. Berger, R., Une nouvelle technique d’analyse du caryotype, Compt. Rend. Acad. Sci. (.Paris) (1971).

    Google Scholar 

  5. Bobrow, M., Collacott, H. E. A. C., and Madan, K., Chromosome banding with acridine orange, Lancet 11: 1311 (1972).

    Article  Google Scholar 

  6. Bobrow, M., Madan, K., and Pearson, P. L., Staining of some specific regions of human chromosomes, particularly the secondary constriction region of no. 9, Nature New Biol. 238: 122 (1972).

    PubMed  CAS  Google Scholar 

  7. Bobrow, M., Pearson, P. L., Pike, M. C., and El Alii, O. S., Length variation in the quinacrine-binding segment of human Y chromosomes of different sizes, Cytogenetics 10: 190.

    Google Scholar 

  8. Carpentier, S., Dutrillaux, B., and Lejeune, J., Effet du milieu ionique sur la de- naturation thermique ménagée des chromosomes humains, Ann. Genet 15: 203 (1972).

    PubMed  CAS  Google Scholar 

  9. Caspersson, T., de la Chapelle, A., Lindsten, J., Schroder, J., and Zech, L., Absence of brightly fluorescent Y material in XX men, Ann. Genet 14: 173 (1971).

    PubMed  CAS  Google Scholar 

  10. Caspersson, T., Farber, S., Foley, G. E., Kudynowski, J., Modest, E. J., Simons- son, E., Wagh, V., and Zech, L., Chemical differentiation along metaphase chromosomes, Exp. Cell Res 49: 219 (1968).

    Article  PubMed  CAS  Google Scholar 

  11. Caspersson, T., Gahrtow, G., Lindsten, J., and Zech, L., Identification of the Philadephia chromosome as a number 22 by quinacrine mustard fluorescence analysis, Expt. Cell Res 63: 238 (1970).

    Article  CAS  Google Scholar 

  12. Caspersson, T., Hulten, M., Lindsten, J., Therkelsen, A. J., and Zech, L., Identification of different Robertsonian translocations in man by quinacrine mustard fluorescence analysis, H er éditas 67: 213 (1971).

    CAS  Google Scholar 

  13. Caspersson, T., Lindsten, J., and Zech, L., Identification of the abnormal B group chromosome in the cri du chat syndrome by Q.M. fluorescence, Exp. Cell Res 61: 475 (1970).

    Google Scholar 

  14. Caspersson, T., Lindsten, J., Zech, L., Buckton, K. E., and Price, W. M., Four patients with trisomy 8 identified by the fluorescence and Giemsa banding techniques, J. Med. Genet 9: 1 (1972).

    Article  PubMed  CAS  Google Scholar 

  15. Caspersson, T., Lomakka, G., and Zech, L., The 24 fluorescence patterns of the human metaphase chromosomes: Distinguishing characters and variability, Here- dit as 67: 89 (1971).

    Google Scholar 

  16. Caspersson, T., Zech, L., Modest, E. J., Foley, G. E., Wagh, V., and Simonsson, E., Chemical differentiation with fluorescent alkylating agents in Vicia faba metaphase chromosomes, Exp. Cell Res 58: 128 (1969).

    Article  PubMed  CAS  Google Scholar 

  17. Caspersson, T., Zech, L., and Johansson, C., Analysis of human metaphase chromosome set by aid of DNA-binding fluorescent agents, Exp. Cell Res 62: 490 (1970).

    Article  PubMed  CAS  Google Scholar 

  18. Caspersson, T., Zech, L., Johansson, C., and Modest, E. J., Identification of human chromosomes by DNA-binding fluorescent agents, Chromosoma 30: 215 (1970).

    Article  PubMed  CAS  Google Scholar 

  19. de la Chapelle, A., Schröder, J., Selander, S. K., and Stenstrand, K., Differences in DNA composition along mammalian metaphase chromosomes, Chromosoma 42: 365 (1973).

    Google Scholar 

  20. Chiarelli, B., and Sarti Chiarelli, M., Bandeggiamento dei cromosomi con tripsina, Riv. Antrop 57: 269 (1971).

    Google Scholar 

  21. Clark, R. J., and Felsenfeld, G., Association of arginine rich histones with G-C- rich regions of DNA in chromatin, Nature New Biol. 240: 226 (1972).

    PubMed  CAS  Google Scholar 

  22. Cohen, M. M., Shaw, M. W., and MacClure, J. W., Racial differences in the length of the human Y chromosome, Cytogenetics 5: 34 (1966).

    Article  PubMed  CAS  Google Scholar 

  23. Comings, D. E., Biochemical mechanisms of chromosome banding and color banding with acridine orange, in: Nobel Symposium 23: Chromosome Identification, pp. 293–299, Nobel Foundation, Stockholm, Academic Press, New York and London (1973).

    Google Scholar 

  24. Couturier, J., Etude d’une technique de marquage des chromosomes humains par action d’enzymes protéolytiques, Thèse Médecine, Paris (1972).

    Google Scholar 

  25. Couturier, J., Dutrillaux, B., and Lejeune, J., Etude des fluorescences spécifiques des bandes R et des bandes Q des chromosomes humains, Compt. Rend. Acad. Sei. (Paris) 276: 339 (1973).

    CAS  Google Scholar 

  26. Distèche, C., Hagemeijer, A., Frederic, J., and Progneaux, D., An abnormal large

    Google Scholar 

  27. human chromosome identified as an end-to-end fusion of two X’s by combined results of the new banding techniques and microdensitometry, Clin. Genet 3: 388 (1972).

    Google Scholar 

  28. Drets, M. E., and Shaw, M. W., Specific banding patterns of human chromosomes, Proc. Natl. Acad. Sci 68: 2073 (1971).

    Article  PubMed  CAS  Google Scholar 

  29. Dutrillaux, B., Nouveau système de marquage chromosomiques: Les bandes T, Chromosoma 41: 395 (1973).

    Article  PubMed  CAS  Google Scholar 

  30. Dutrillaux, B., Sur deux méthodes de marquage des chromosomes humains: Mise en évidence des bandes R et des bandes T, Rev. Med. Chir. Iasi 2 :329 (1973).

    Google Scholar 

  31. Dutrillaux, B., Chromosomal aspects of human male sterility, in: Nobel Symposium 23: Chromosome Identification, pp. 205 - 208, Nobel Foundation, Stockholm, Academic Press, New York and London (1973).

    Google Scholar 

  32. Dutrillaux, B., Application to the normal karyotype of R-band and G-band techniques involving proteolytic digestion, in: Nobel Symposium 23: Chromosome Identification, Nobel Foundation, Stockholm, Academic Press, New York and London (1973).

    Google Scholar 

  33. Dutrillaux, B., New techniques in the study of human chromosomes, in: Proceedings of the Fourth International Conference on Birth Defects, pp. 59–70, Excerpta Medica, Amsterdam (1973).

    Google Scholar 

  34. Dutrillaux, B., and Couturier, J., Techniques d’analyses chromosomiques, in: Biologie Clinique, pp. 5-12, l’Expansion, Paris (1972).

    Google Scholar 

  35. Dutrillaux, B., Couturier, J., Rotman, J., Salat, J., and Lejeune, J., Stérilité et translocation familiale t(lq-; Xq +), Compt. Rend. Acad. Sci. (Paris) 274: 3324 (1972).

    CAS  Google Scholar 

  36. Dutrillaux, B., Finaz, C., de Grouchy, J., and Lejeune, J., Comparison of banding patterns of human chromosomes obtained with heating, fluorescence, and proteolytic digestion, Cytogenetics 2: 113 (1972).

    Article  Google Scholar 

  37. Dutrillaux, B., de Grouchy, J., Finaz, C., and Lejeune, J., Mise en évidence de la structure fine des chromosomes humains par digestion enzymatique (pronase en particulier), Compt. Rend. Acad. Sci. (Paris) 273: 587 (1971).

    CAS  Google Scholar 

  38. Dutrillaux, B., Jonasson, J., Kertin, L., Lejeune, J., Lindsten, J., Petersen, G. B., and Saldana-Garcia, P., An unbalanced 4q/21q translocation identified by the R, but not by the G and O chromosome banding techniques, Ann. Genet 16: 11 (1973).

    PubMed  CAS  Google Scholar 

  39. Dutrillaux, B., Laurent, C., Couturier, J., and Lejeune, J., Coloration par l’acridine orange de chromosomes préalablement traités par le.5-bromodéoxyuridine (BUDR), Compt. Rend. Acad. Sci. (Paris) 276: 3179 (1973).

    CAS  Google Scholar 

  40. Dutrillaux, B., Laurent, C., Robert, J. M., and Lejeune, J., Inversion péricentrique inv (10), chez la mère, et aneusomie de recombinaison rec (10), inv (10) chez son fils, Cytogenetics 12: 245 (1973).

    Article  CAS  Google Scholar 

  41. Dutrillaux, B., and Lejeune, J., Analyse de la descendance des porteurs d’une translocation t(21qDq), Ann. Genet 12: 77 (1969).

    PubMed  CAS  Google Scholar 

  42. Dutrillaux, B., and Lejeune, J., Sur une nouvelle technique d’analyse du caryotype humain, Compt. Rend. Acad. Sci. (Paris) 272: 2638 (1971).

    CAS  Google Scholar 

  43. Dutrillaux, B., and Lejeune, J., Sur une nouvelle technique d’analyse du caryotype humain, Excerpta Med. Int. Congr. Ser 233: 61 (1971).

    Google Scholar 

  44. Dutrillaux, B., and Lejeune, J., unpublished data.

    Google Scholar 

  45. Dutrillaux, B., Rethoré, M. O., and Lejeune, J., Analysis of t(Dq Dq) translocations after heat denaturation, Chrom. Inf. Serv. (Japan) 14: 3 (1973).

    Google Scholar 

  46. Dutrillaux, B., Rethoré, M. O., Prieur, M., Couturier, J., Carpentier, S., and Lejeune, J., New techniques of chromosome banding: Application to translocation analysis, in: Proceedings of the International Congress BRNO (1972).

    Google Scholar 

  47. Dutrillaux, B., Rethoré, M. O., Prieur, M., Raoul, O., Berger, R., and Lejeune, J., Reconnaissance des chromosomes du groupe G par la méthode de dénaturation ménagée, Exp. Cell Res 70: 453 (1972).

    Google Scholar 

  48. Finaz, C., and de Grouchy, J., Le caryotype humain après traitment par Pa-chymo- trypsine, Ann. Genet 14: 309 (1971).

    PubMed  CAS  Google Scholar 

  49. Forabosco, A., and Dutrillaux, B., unpublished data.

    Google Scholar 

  50. Forabosco, A., Dutrillaux, B., and Couturier, J., unpublished data.

    Google Scholar 

  51. Forabosco, A., Dutrillaux, B., Toni, G., and Lejeune, J., Enfant trisomique 21 libre et translocation t(14q22q) maternelle, Ann. Genet 16: 57 (1973).

    PubMed  CAS  Google Scholar 

  52. Fraccaro, M., Scappaticci, S., Tiepolo, L., and Turpini, R., Identification of a structurally abnormal Y chromosome, Ann. Genet 14: 53 (1971).

    PubMed  CAS  Google Scholar 

  53. Gagné, R., and Laberge, C., Specific cytological recognition of the hterochromatic segment of number 9 chromosome in man, Exp. Cell Res 73: 239 (1972).

    Article  PubMed  Google Scholar 

  54. Genest, P., Laberge, C., Poty, J., Gagné, R., and Bouchard, M., Transmission d’un petit Y durant onze générations dans une lignée familiale, Ann. Genet 13: 233 (1970).

    PubMed  CAS  Google Scholar 

  55. German, J., Lejeune, J., Mclntyre, M., and de Grouchy, J., Chromosomal autoradiography in the cri du chat syndrome, Cytogenetics, 3: 347 (1964).

    Article  Google Scholar 

  56. de Grouchy, J., Finaz, C., Roubin, M., and Roy, J., Deux translocations familiales survenues ensemble chez chacune de deux soeurs, l’une équilibrée, l’autre trisomique partielle lOq, Ann. Genet 15: 85 (1972).

    PubMed  Google Scholar 

  57. de Grouchy, J., Turleau, C., and Leonard, C., Etude en fluorescence d’une trisomie C mosaïque, probablement 8 46, XY/47, XY, ?8 +, Ann. Genet 14: 69 (1971).

    PubMed  Google Scholar 

  58. de Grouchy, J., Turleau, C., Roubin, M., and Klein, M., Evolutions caryotypiques de l’homme et du chimpanzé: Etude comparative des topographies de bandes après dénaturation ménagée, Ann. Genet 15: 79 (1972).

    PubMed  Google Scholar 

  59. Grace, E., Sutherland, G. R., and Bain, A. D., Familial insertional translocation, Lancet 11: 231 (1972).

    Article  Google Scholar 

  60. Gray, J. E., Syrett, J. E., Ritchie, K. M., and Elliott, W. D., An interstitial translocation: Chromosome no. lp to 4q, Lancet ii: 92 (1972).

    Google Scholar 

  61. Jones, K. W., Chromosomal and nuclear location of mouse satellite DNA in individual cells, Nature 225: 912 (1970).

    Article  PubMed  CAS  Google Scholar 

  62. Jones, K. W., and Corneo, G., Location of satellite and homogeneous DNA sequences on human chromosomes, Nature New Biol. 233: 268 (1971).

    Article  PubMed  CAS  Google Scholar 

  63. Laurent, C., Dutrillaux, B., and Binder, P., Application de la méthode de dénaturation ménagée: Dénaturation de préparations colorées antérieurement, Ann. Genet 15: 201 (1972).

    PubMed  CAS  Google Scholar 

  64. Laurent, C., Robert, J. M., Grambert, J., and Dutrillaux, B., Observations cliniques et cytogénétiques de deux adultes trisomiques C en mosaïque: Individualisation du chromosome surnuméraire par la technique moderne de dénaturation: 47, XY, ?8 +, Lyon Med. 226: 827 (1971).

    PubMed  CAS  Google Scholar 

  65. Lejeune, J. and Berger, R., Sur deux observations familiales de translocations, complexes, Ann. Genet 8: 21 (1965).

    PubMed  CAS  Google Scholar 

  66. Lejeune, J., unpublished data.

    Google Scholar 

  67. Lejeune, J., Dutrillaux, B., Lafourcade, J., Berger, R., Abonyi, D., and Rethoré, M. O., Endroreduplication sélection du bras long du chromosome 2 chez une femme et sa fille, Compt. Rend. Acad. Sci. (Paris) 226: 24 (1968).

    Google Scholar 

  68. Lejeune, J., Dutrillaux, B., Rethoré, M. O., and Prieur, M., Comparaison de la structure fine des chromatides d’Homo sapiens et de Pan-troglodytes, Chromosoma 43: 423 (1973).

    Google Scholar 

  69. Lejeune, J., Dutrillaux, B., Rethoré, M. O., Prieur, M., Couturier, J., Carpentier, S., and Raoul, O., Analysis of 30 cases of translocation by the controlled heat dénaturation, in: Modern Aspects of Cytogenetics: Constitutive Heterochromatin in Man, Symposia Medica Hoechst 6, pp. 191–200, F. K. Schattauer, Stuttgart and New York (1972).

    Google Scholar 

  70. Lejeune, J., Gautier, M., and Turpin, R., Les chromosomes humains en culture de tissus, Compt. Rend. Acad. Sei. (Paris) 248: 602 (1959).

    CAS  Google Scholar 

  71. Lejeune, J., and Rethoré, M. O., Trisomies of chromosome no. 8, in: Nobel Symposium 23: Chromosome Identification, pp. 214 - 216, Nobel Foundation, Stockholm, Academic Press, New York and London (1973).

    Google Scholar 

  72. Lejeune, J., Rethoré, M. O., Dutrillaux, B., and Martin, G., Translocation 8-22 sans changement de longueur et trisomie partielle 8q, Exp. Cell Res 74: 293 (1972).

    Article  PubMed  CAS  Google Scholar 

  73. Lubs, H. A., McKenzie, W. H., and Merrick, S., Comparative methodology and mechanisms of banding, in: Nobel Symposium 23: Chromosome Identification, pp. 61 - 76, Nobel Foundation, Stockholm, Academic Press, New York and London (1973).

    Google Scholar 

  74. Marushiga, K., and Bonner, J., Template properties of liver chromatin, /. Mol. Biol 15: 160 (1966).

    Article  Google Scholar 

  75. Miller, O. J., Miller, D. A., Allderdice, P. W., Dev, V. G., and Grewall, M. S., Quinacrine fluorescence karyotypes of human diploid and heteroploid cell lines, Cytogenetics 10: 338 (1971).

    Article  PubMed  CAS  Google Scholar 

  76. Miller, O. J., Schreck, R. R., Beiser, S. M., and Erlanger, B. F., Immunofluorescent studies of chromosome banding with antinucleoside antibodies, in: Nobel Symposium 23: Chromosome Identification, pp. 43 - 48, Nobel Foundation, Stockholm, Academic Press, New York and London (1973).

    Google Scholar 

  77. Nieburh, E., Dicentric and Monocentric Robertsonian translocations in man, Humangenetik 16: 217 (1972).

    Article  Google Scholar 

  78. Niebuhr, E., Localization of the deleted segment in the cri du chat syndrome, Humangenetik 16: 357 (1972).

    PubMed  CAS  Google Scholar 

  79. No well, P. C., and Hungerford, D. A., A minute chromosome in human granulocytic leukemia, Science 132: 1497 (1960).

    Google Scholar 

  80. Ohno, S., and Cattanach, B. M., Cytological study of an X autosome translocation in Mus mus cuius, Cytogenetics 1: 129 (1962).

    CAS  Google Scholar 

  81. Pachmann, U., and Rigler, R., Quantum yield of acridines interacting with DNA of defined base sequence, Exp. Cell Res 72: 602 (1972).

    Article  PubMed  CAS  Google Scholar 

  82. Palmer, C. G., 5-Bromodeoxyuridine induced constrictions in human chromosomes, Can. J. Genet. Cytol 12: 816 (1970).

    PubMed  CAS  Google Scholar 

  83. Pardue, M. L. and Gall, J. G., Chromosomal localization of mouse satellite DNA, Science 168: 1356 (1970).

    Article  PubMed  CAS  Google Scholar 

  84. Paris Conference, 1971, Standardization in Human Cytogenetics. Birth Defects: Original Article Series, Vol. 8, No. 7, National Foundation, New York (1972).

    Google Scholar 

  85. Patil, S. R., Mernick, S., and Lubs, H. A., Identification of each human chromosome with a modified Giemisa stain, Science 173: 821 (1971).

    Article  PubMed  CAS  Google Scholar 

  86. Pearson, P. L., A fluorescent technique for identifying human chromatin in a variety of tissues, Bull. Europ. Soc. Hum. Genet 4: 35 (1970).

    Google Scholar 

  87. Prieur, M., Dutrillaux, B., and Lejeune, J., Planches descriptives des chromosomes humains (Analyse en bandes R et nomenclature selon la conférence de Paris 1971), Ann. Genet 16: 39 (1973).

    PubMed  CAS  Google Scholar 

  88. Rethoré, M. O., Dutrillaux, B., Baheux, G., Gerveaux, J., and Lejeune, J., Monosomie pour les régions juxtacentromeriques d’un chromosome 21, Exp. Cell Res 70: 455 (1972).

    Google Scholar 

  89. Rethoré, M. O., Hoehn, M., Rott, H. D., Couturier, J., Dutrillaux, B., and Lejeune, J., Analyse de la trisomie 9p par dénaturation ménagée, a propos d’un nouveau cas, Humangenetik 18: 129 (1973).

    Article  PubMed  Google Scholar 

  90. Rethoré, M. O., and Lafourcade, J., Maladie du cri du chat et syndrôme 4p -, Excerpta Med. Int. Congr. Ser, 233: 150 (1971).

    Google Scholar 

  91. Rethoré, M. O., Larget-Piet, L., Abonyi, D., Boeswillwald, M., Berger, R., Carpentier, S., Cruveiller, J., Dutrillaux, B., LaFourcade, J., Penneau, M., and Lejeune, J., Sur quatre cas de trisomie pour le bras court du chromosome 9, individualisation d’une nouvelle entité morbide, Ann. Genet 13: 217 (1970).

    PubMed  Google Scholar 

  92. Rethoré, M. O., Lejeune, J., Carpentier, S., Prieur, M., Dutrillaux, B., Seringe, P., Rossier, A., and Job, J. C., Trisomie pour la partie distale du chromosome 3 chez trois germains. Premier exemple d’insertion chromosomique: ins (7; 3) (q31; p21p26), Ann. Genet 15: 159 (1972).

    PubMed  Google Scholar 

  93. Rigler, R., Microfluorometry characterization of intracellular nucleic acids and nucleoproteins by acridine orange, Acta Physiol. Scand. 67: 1 (Suppl. 267) (1966).

    Google Scholar 

  94. Robinson, J. A., and Buckton, K. E., Quinacrine fluorescence of variant and abnormal human Y chromosomes, Chromosoma 35: 342 (1971).

    Article  PubMed  CAS  Google Scholar 

  95. Rowley, J. D., A new consistent chromosomal abnormality in chronic myelogenous leukemia identified by quinacrine fluorescence and giemsa staining, Nature 243: 290 (1973).

    Article  PubMed  CAS  Google Scholar 

  96. Saunders, G. F., Hsu, T. C., Getz, H. J., Simes, E. L., and Arrighi, F. E., Locations of human satellite DNA in human chromosomes, Nature New Biol. 236: 244 (1972).

    Article  CAS  Google Scholar 

  97. Schnedl, W., Banding pattern of human chromosomes, Nature New Biol. 233: 93 (1971).

    PubMed  CAS  Google Scholar 

  98. Seabright, M., A rapid banding technique for human chromosomes, Lancet 11: 971 (1971).

    Article  Google Scholar 

  99. Seabright, M., High resolution studies on the pattern of induced exchanges in the human karyotype, Chromosoma 40: 333 (1973).

    Article  PubMed  CAS  Google Scholar 

  100. Seleznev, Y. V., A modified method of Giemsa staining of human chromosomes to reveal their linear differentiation, Ann. Genet 16: 139 (1973).

    PubMed  CAS  Google Scholar 

  101. Shiraishi, Y., and Yosida, T. H., Banding pattern analysis of human chromosomes by use of a urea treatment technique, Chromosoma 37: 75 (1972).

    Article  PubMed  CAS  Google Scholar 

  102. Sumner, A. T., Evans, H. J., and Buckland, R. A., A new technique for distinguishing between human chromosomes, Nature New Biol. 232: 31 (1971).

    PubMed  CAS  Google Scholar 

  103. Therkelsen, A. J., Myhre Jensen, O., Jonasson, J., Lamm, L. U., Lauritzen, J. G., Lindsten, J., and Bruun Petersen, G., Studies on spontaneous abortions, in: Nobel Symposium 23: Chromosome Identification, pp. 251–257, Nobel Foundation, Stockholm, Academic Press, New York and London (1973).

    Google Scholar 

  104. Utakoji, T., Differential staining patterns of human chromosomes treated with potassium permanganate, Nature 239: 168 (1972).

    Article  PubMed  CAS  Google Scholar 

  105. Venuat, A. M., Dutrillaux, B., Rosenfeld, C., Paintrand, M., and Lejeune, J., Etude cytogénétique d’une lignée permanente de leucocytes humains par la méthode de dénaturation ménagée, Compt. Rend. Acad. Sci. (Paris) 274: 3438 (1972).

    CAS  Google Scholar 

  106. Wang, H. C., and Fedoroff, S., Banding in human chromosomes treated with trypsin, Nature New Biol. 235: 52 (1972).

    Article  PubMed  CAS  Google Scholar 

  107. Weisblum, B., and de Haseth, P. L., Quinacrine, a chromosome stain specific for deoxyadenylate-deoxythymidinate-rich regions in DNA, Proc. Natl. Acad. Sci. 69: 629 (1972).

    Google Scholar 

  108. Yunis, J J., Roldan, L., Yasmineh, W. G., and Lee, J. C., Staining of satellite DNA in metaphase chromsomes, Nature 231: 532 (1971).

    Article  PubMed  CAS  Google Scholar 

  109. Zakharov, A. F., Seleznev, J. V., Benjusch, V. A., Baranovskaya, L. I., and Demintseva, V. I., Differentiation along human chromosomes in relation to their identification, Excerpta Med. Int. Congr. Ser 233: 193 (1971).

    Google Scholar 

  110. Zech, L., Investigation of metaphase chromosomes with DNA binding fluoro- chromes, Exp. Cell Res 58: 463 (1969).

    Google Scholar 

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Dutrillaux, B., Lejeune, J. (1975). New Techniques in the Study of Human Chromosomes: Methods and Applications. In: Harris, H., Hirschhorn, K. (eds) Advances in Human Genetics. Advances in Human Genetics, vol 5. Springer, Boston, MA. https://doi.org/10.1007/978-1-4615-9068-2_2

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