Variability in serologically detected male antigen titer and some resulting problems: A critical review Maria Teresa ZenzesT. Edward Reed Review Articles Pages: 103 - 109
Comments on the paper by M. T. Zenzes and T. E. Reed hum genet 66:103–109 (1984) Antonia MayerováU. MüllerM. Fraccaro OriginalPaper Pages: 110 - 112
Reply to the comments by Mayerová, Müller, Wiberg, Wolf, and Fraccaro Hum Genet 66:110–112 Maria Teresa ZenzesT. Edward Reed OriginalPaper Pages: 113 - 114
The current state of research with peripheral tissues in Huntington disease G. C. Beverstock Review Articles Pages: 115 - 131
Karyotyping and identification of human chromosome polymorphisms by single fluorochrome flow cytometry D. K. GreenJudith A. FantesH. J. Evans Original Investigations Pages: 143 - 146
Heterocellular hereditary persistence of fetal hemoglobin (HPFH). Molecular mechanisms of abnormal γ-gene expression in association with β thalassemia and linkage relationship with the β-globin gene cluster A. GiampaoloF. MavilioM. Marinucci Original Investigations Pages: 151 - 156
Non-random in vitro 7;14 translocations detected in a routine cytogenetic series. 12 Examples and their possible significance C. WallaceR. BernsteinM. R. Pinto Original Investigations Pages: 157 - 161
Chromosome studies in 496 infertile males with a sperm count below 10 million/ml A. E. RetiefJ. A. Van ZylJ. Brusnický Original Investigations Pages: 162 - 164
Familial inv(1)(p3500q21.3) associated with azoospermia H. RiveraM. C. Alvarez-ArratiaJ. M. Cantú Original Investigations Pages: 165 - 167
Differential enzyme activities in human esterase D phenotypes S. HoraiE. Matsunaga Original Investigations Pages: 168 - 170
A new glucose-6-phosphate dehydrogenase variant (G-6-PD Kalyan) found in a Koli family C. S. IshwadS. N. Naik Original Investigations Pages: 171 - 175
Meiotic configurations in female trisomy 21 foetuses R. M. Speed Original Investigations Pages: 176 - 180
Regional mapping of catalase and Wilms tumor—aniridia, genitourinary abnormalities, and mental retardation triad loci to the chromosome segment 11p1305→p1306 K. NaraharaK. KikkawaK. Matsuoka Original Investigations Pages: 181 - 185
A decreasing tendency for cytogenetic abnormality in peripheral lymphocytes of retinoblastoma patients with 13q14 deletion mosaicism T. MotegiK. Minoda Original Investigations Pages: 186 - 189
Assignment of human phosphoribosylglycinamide synthetase locus to region 21q221 B. ChadefauxD. AllardH. Jérôme Original Investigations Pages: 190 - 192
Chromosomal abnormalities in human sperm: Comparisons among four healthy men B. BrandriffL. GordonA. Wyrobek Original Investigations Pages: 193 - 201
Assignment of the gene for uroporphyrinogen decarboxylase to human chromosome 1 by somatic cell hybridization and specific enzyme immunoassay H. de VerneuilB. GrandchampY. Nordmann Original Investigations Pages: 202 - 205
Localization of a gene which complements branched-chain amino acid transaminase deficiency to the short arm of human chromosome 12 Carol JonesEmma E. Moore Original Investigations Pages: 206 - 211
The use of fructose 1-phosphate to detect Hunter heterozygotes in fibroblast cultures from high-risk carriers T. Tønnesen Original Investigations Pages: 212 - 216
Restriction site polymorphism in the phosphoglycerate kinase gene on the X chromosome Mara H. HutzA. M. MichelsonH. H. Kazazian Jr. Original Investigations Pages: 217 - 219
Synchronization of human leukemic cells: Relevance for high-resolution chromosome banding J. H. GalloJ. V. OrdonezJ. R. Testa Original Investigations Pages: 220 - 224
Cytogenetic investigations in mentally retarded and normal males from 14 families with the fragile site at Xq28 Karen Brøndum NielsenN. Tommerup Original Investigations Pages: 225 - 229
Regional mapping of clotting factors VII and X to 13q34. Expression of factor VII through chromosome 8 J. de GrouchyMarie-Dominique DautzenbergFrançoise Chavin-Colin Original Investigations Pages: 230 - 233
Estimation of aneuploidy levels in human spermatozoa using chromosome specific probes and in situ hybridisation A. M. JosephJ. R. GosdenA. C. Chandley Original Investigations Pages: 234 - 238
Sequence of centromere separation another mechanism for the origin of nondisjunction B. K. Vig Original Investigations Pages: 239 - 243
Genetic analysis of human lymphocyte proteins by two-dimensional gel electrophoresis: I. KondoK. YamakawaH. Hamaguchi Original Investigations Pages: 244 - 247
Genetic analysis of human lymphocyte proteins by two-dimensional gel electrophoresis: I. KondoT. YamamotoH. Hamaguchi Original Investigations Pages: 248 - 251
Diagnostic application of first trimester trophoblast sampling in 100 pregnancies G. SimoniB. BrambatiM. Fraccaro Original Investigations Pages: 252 - 259
Familial congenital esophageal atresia M. Van StaeyS. De BieJ. De Roose Original Investigations Pages: 260 - 266
Complete pachytene chromomere karyotypes of human spermatocyte bivalents J. M. LucianiM. R. GuichaouaM. R. Morazzani Original Investigations Pages: 267 - 271
A sensitive and dependable assay for distinguishing hamster and human X-linked steroid sulfatase activity in somatic cell hybrids H. F. WillardMaria Tzetis Holmes Original Investigations Pages: 272 - 275
Gd(-) Gifu and Gd(-) Fukuoka. Two new variants of glucose-6-phosphate dehydrogenase found in Japan H. FujiiS. MiwaJ. Okamura Original Investigations Pages: 276 - 278
Genetic polymorphism of the seventh component of complement in a Japanese population S. NakamuraO. OoueK. Abe Original Investigations Pages: 279 - 281
Siblings with renal tubular acidosis and nerve deafness. The first family in Japan Takanobu AnaiJiro YamamotoBunsaku Nagai Clinical Case Reports Pages: 282 - 285
Smaller autosomal C band sizes in blacks than in caucasoids R. ZamengaM. S. MatteviB. Erdtmann Letters to the Editors Pages: 286 - 286
