A proposed growth regulatory function for the serologically detectable sex-specific antigen H-Ys Barbara F. HeslopMark P. BradleyMargaret A. Baird Review Article Pages: 99 - 104
A genetic and anthropological study of atlanto-occipital fusion A. K. KallaS. KhannaF. Vogel Original Investigations Pages: 105 - 112
Isolation of chromosome-21-specific DNA probes and their use in the analysis of nondisjunction in Down syndrome J. GaltE. BoydM. A. Ferguson-Smith Original Investigations Pages: 113 - 119
Hypohidrotic ectodermal dysplasia Simone GilgenkrantzClaudine Blanchet-BardonY. Alembik Original Investigations Pages: 120 - 122
Ferritin H gene polymorphism in idiopathic hemochromatosis Véronique DavidPanos PapadopoulosMarcel Simon Original Investigations Pages: 123 - 126
Centromeric association of a microchromosome M. SchmidT. HaafM. Meurer Original Investigations Pages: 127 - 136
Centromeric association and non-random distribution of centromeres in human tumour cells T. HaafM. Schmid Original Investigations Pages: 137 - 143
Localization of Y chromosome sequences and X chromosomal replication studies in XX males W. SchemppG. MüllerU. Wolf Original Investigations Pages: 144 - 148
The gene for the Lp(a)-specific glycoprotein is closely linked to the gene for plasminogen on chromosome 6 Gisela LindahlElisabeth GersdorfGerd Utermann Original Investigations Pages: 149 - 152
Chromosomal assignment of a glutamic acid transfer RNA (tRNAGlu) gene to 1p36 E. BoydA. TheriaultJ. M. Connor Original Investigations Pages: 153 - 156
Localization of the coagulation factor XIII B subunit gene (F13B) to chromosome bands 1q31–32.1 and restriction fragment length polymorphism at the locus G. C. WebbM. CogganP. g. Board Original Investigations Pages: 157 - 160
Chronic nonspherocytic hemolytic anemia (CNSHA) and glucose 6 phosphate dehydrogenase (G6PD) deficiency in a patient with familial amyloidotic polyneuropathy (FAP) Joan Lluis Vives-CorronsM. Assumpció PujadesAnna Merino Original Investigations Pages: 161 - 164
Ataxia-telangiectasia fibroblasts have less fibronectin mRNA than control cells but have the same levels of integrin and β-actin mRNA Yechiel BeckerEynat TaborYael Asher Original Investigations Pages: 165 - 170
The human cytochrome P450 CYP3 locus: assignment to chromosome 7q22-qter Nigel K. SpurrAlan C. GoughC. Roland Wolf Original Investigations Pages: 171 - 174
Phytanic acid alpha-oxidation and complementation analysis of classical Refsum and peroxisomal disorders Bwee Tien Poll-TheOla H. SkjeldalJean-Marie Saudubray Original Investigations Pages: 175 - 181
H-Y antigenicity of human fibroblasts C. JorgensenE. J. Eichwald Short Communications Pages: 182 - 182
Confirmation of linkage disequilibrium between haplotype B (XV-2c, allele 1; KM-19, allele 2) and cystic fibrosis allele in the French population M. VidaudA. KitzisJ. C. Kaplan Short Communications Pages: 183 - 184
Erythrocyte acid phosphatase (ACP1) activity N. LucariniP. BorgianiE. Bottini Short Communications Pages: 185 - 187
Presymptomatic testing for Huntington's disease Ann CurtisF. MillanD. J. H. Brock Short Communications Pages: 188 - 190
Sublocalization of the human protein C gene on chromosome 2q13–q14 P. PatracchiniV. AielloF. Bernardi Short Communications Pages: 191 - 192
Detection of Duchenne muscular dystrophy carriers by dosage analysis using the DMD cDNA clone 8 Yiping MaoMarion Cremer Short Communications Pages: 193 - 195
Familial transmission of 16p trisomy in an infant S. M. JalalDonald W. DayJim Rogers Clinical Case Report Pages: 196 - 198
Recombination between DXS7, DXS84 and a rare form of X-linked retinitis pigmentosa (McK-30 320) Diana CurtisC. E. Blank Letter to the Editors Pages: 200 - 202
