Genetic polymorphism of human plasma α1-B-glycoprotein: phenotyping by immunoblotting or by a simple method of 2-D electrophoresis B. GahneR. K. JunejaA. Stratil Original Investigations Pages: 111 - 115
Chromosome analysis of spermatozoa from a male heterozygous for a 13;14 Robertsonian translocation F. PellestorB. SeleH. Jalbert Original Investigations Pages: 116 - 120
Localization of the ornithine aminotransferase gene and related sequences on two human chromosomes Vijaya RameshRoger EddyJames F. Gusella Original Investigations Pages: 121 - 126
A new Hind III restriction fragment length polymorphism in the hemophilia A locus P. AhrensT. A. KruseN. Din Original Investigations Pages: 127 - 128
The potential of family flow karyotyping for the detection of chromosome abnormalities P. HarrisA. CookeM. A. Ferguson-Smith Original Investigations Pages: 129 - 133
Variation in the expression of aphidicolin-induced fragile sites in human lymphocyte cultures Ann P. Craig-HolmesLouise C. StrongSen Pathak Original Investigations Pages: 134 - 137
Increased concentrations of various amino acids in schizophrenic patients E. SmeraldiA. LuccaL. Bellodi Original Investigations Pages: 138 - 140
Spermatogenesis in two patients with the fragile X syndrome R. JohannissonH. RehderE. Schwinger Original Investigations Pages: 141 - 147
Selection of human cells having two different types of mutations in individual cells (genetic/artificial mutants) Naoyuki KamataniShoko KuroshimaKusuki Nishioka Original Investigations Pages: 148 - 152
Three cases of 45,X/46,XYnf mosaicism Dorothee Gänshirt-AhlertIvar Harry PawlowitzkiAndreas Gal Original Investigations Pages: 153 - 156
Application of cloned satellite DNA sequences to molecular-cytogenetic analysis of constitutive heterochromatin heteromorphisms in man Yuri B. YurovS. P. MitkevichI. A. Alexandrov Original Investigations Pages: 157 - 164
Ten families with fragile X syndrome: linkage relationships with four DNA probes from distal Xq Julie A. BuchananKarin E. BucktonNicholas Hastie Original Investigations Pages: 165 - 172
Study of human chromosome V Shio Jean LinChristine FigueiredoMing-liang Lee Original Investigations Pages: 173 - 175
Cytogenetic studies using Q-band polymorphisms in patients with AML receiving marrow from like-sex donors M. T. KhokharSylvia D. LawlerJ. L. Millar Original Investigations Pages: 176 - 180
The clastogenic effect of 5-methoxypsoralen plus UV-A in human lymphocytes in vitro and its modification by the anticlastogen β-aminoethylisothiouronium Gudrun AbelAnnette Mannschedel Original Investigations Pages: 181 - 185
Exclusion of the Friedreich ataxia gene from chromosome 19 S. ChamberlainC. S. WorrallR. Williamson Original Investigations Pages: 186 - 190
The gene coding for the human T-lymphocyte CD2 antigen is located on chromosome 1p Marion H. BrownPatricia A. GormanMichael J. Crumpton Original Investigations Pages: 191 - 195
α-Thalassemia in Saudi Arabia: deletion pattern M. A. F. El-Hazmi Original Investigations Pages: 196 - 198
Three new G6PD variants, G6PD Adana, G6PD Samandağ, and G6PD Balcali in Çukurova, Turkey Kiymet AksoyGüneş T. YüregirIsa Ünlükurt Short Communication Pages: 199 - 201
Chromosome deletion at 11q23 in an abnormal child from a family with inherited fragility at 11q23 L. E. VoullaireG. C. WebbM. A. Leversha Clinical Case Report Pages: 202 - 204
De novo 10q(q21q22) interstitial deletion G. GloverJ. GabarrónJ. A. López Ballester Cases Observed Pages: 205 - 205
Autosomal dominant inheritance of benign bilateral acromial dimples K. MéhesVeronika Meggyessy Cases Observed Pages: 206 - 206
