Psychological issues in genetic counselling Maria ReifHelmut Baitsch Review Articles Pages: 193 - 199
Genetic analysis of carbamyl phosphate synthetase I deficiency Eric R. FearonRichard L. MalloneeLorne T. Kirby Original Investigations Pages: 207 - 210
Genetic polymorphism of complement component C8 S. RogdeB. MevågB. Olaisen OriginalPaper Pages: 211 - 216
Human lens γ-crystallin sequences are located in the p12-qter region of chromosome 2 J. T. den DunnenR. J. E. JongbloedJ. G. G. Schoenmakers Original Investigations Pages: 217 - 221
Two-dimensional gel studies of genetic variation in the plasma proteins of Amerindians and Japanese Jun-ichi AsakawaNorio TakahashiJames V. Neel Original Investigations Pages: 222 - 230
Mapping genetic systems by the supratype method N. E. MortonR. Lew Original Investigations Pages: 231 - 235
DNA semi-conservative synthesis in normal and Fanconi anemia fibroblasts following treatment with 8-methoxypsoralen and near ultraviolet light or with X-rays E. MoustacchiC. Diatloff-Zito Original Investigations Pages: 236 - 242
Mitomycin C-induced mosaicism in C-band regions of human chromosomes 1, 9, 16, and Y Silvana Simi Original Investigations Pages: 243 - 245
Linkage studies of X-linked mental retardation: High frequency of recombination in the telomeric region of the human X chromosome (fragile site/linkage/recombination/X chromosome) K. E. DaviesM. G. MatteiM. E. Pembrey Original Investigations Pages: 249 - 255
Frequency of consanguineous marriages among parents and grandparents of Down patients Marcella DevotoLetizia ProsperiG. Romeo Original Investigations Pages: 256 - 258
The second human calcitonin/CGRP gene is located on chromosome 11 J. W. M. HöppenerP. H. SteenberghC. J. M. Lips Original Investigations Pages: 259 - 263
Spontaneous 6-thioguanine-resistant lymphocytes in Fanconi anemia patients and their heterozygous parents VijavalaxmiE. WunderT. M. Schroeder Original Investigations Pages: 264 - 270
The apolipoprotein CII gene: Subchromosomal localisation and linkage to the myotonic dystrophy locus D. J. ShawA. L. MeredithP. S. Harper Original Investigations Pages: 271 - 273
Variant of ataxia-telangiectasia with low-level radiosensitivity M. FiorilliA. AntonelliP. Petrinelli Original Investigations Pages: 274 - 277
Gc (vitamin D binding protein) subtypes in rheumatoid arthritis S. S. PapihaB. Pal Short Communication Pages: 278 - 280
A familial X-autosome translocation with the breakpoint in the “critical region” U. DiedrichI. Hansmann Clinical Case Reports Pages: 281 - 283
9p trisomy/18p distal monosomy and multiple cutaneous leiomyomata J. P. FrynsM. HaspeslaghH. van Den Berghe Clinical Case Reports Pages: 284 - 286
Complex translocation in habitual abortion A. SmithG. den DulkW. Birrell Cases Observed Pages: 287 - 287
Congenital aplasia of the vasa deferentia of autosomal recessive inheritance in two unrelated sib-pairs A. Czeizel Cases Observed Pages: 288 - 288
High-resolution studies in patients with aniridia-Wilms tumor association Y. NakagomeN. Nagahara Letters to the Editors Pages: 289 - 289
