Nuclear architecture of human pachytene spermatocytes: quantitative analysis of associations between nucleolar and XY bivalents Soledad BerriosRaúl Fernández-Donoso Original Investigations Pages: 103 - 116
Defective, deleted or converted CYP21B gene and negative association with a rare restriction fragment length polymorphism allele of the factor B gene in congenital adrenal hyperplasia N. GhanemJ. M. LobaccaroG. Lefranc Original Investigations Pages: 117 - 125
The 60 and 63 kDa proteolytic peptides of the red cell membrane band-3 protein: their prevalence in human and non-human primates Marcos PalatnikMaria Lucia Marti da Silva SimõesNanci Souto Maior Laranjeira Original Investigations Pages: 126 - 130
In search of a genetic basis for the Rett syndrome Paulo S. MartinhoPriscila G. OttoClaudette Hajaj Gonzalez Original Investigations Pages: 131 - 134
The human MyoD1 (MYF3) gene maps on the short arm of chromosome 11 but is not associated with the WAGR locus or the region for the Beckwith-Wiedemann syndrome M. GesslerH. HameisterH. H. Arnold Original Investigations Pages: 135 - 138
Sex ratio of the mutation frequencies in haemophilia A: estimation and meta-analysis F. R. RosendaalA. H. J. T. Bröcker-VriendsE. Briët Original Investigations Pages: 139 - 146
Cytogenetic and molecular analysis of a Yq isochromosome Martina GuttenbachUlrich MüllerMichael Schmid Original Investigations Pages: 147 - 150
Partial complementation of the Fanconi anemia defect upon transfection by heterologous DNA C. Diatloff-ZitoF. RosselliE. Moustacchi Original Investigations Pages: 151 - 161
Infertility in human males with autosomal translocations: meiotic study of a 14;22 Robertsonian translocation M. R. GuichaouaB. QuackJ. M. Luciani Original Investigations Pages: 162 - 166
Assignment of human tracheobronchial mucin gene(s) to 11p15 and a tracheobronchial mucin-related sequence to chromosome 13 Nguyen Van CongJ. P. AubertJ. Frézal Original Investigations Pages: 167 - 172
Translocation t(1;17)(q12;q25) with a clinical picture like of a proximal deletion of 1q: identification by in situ hybridization with chromosome 1-specific satellite DNA probes Swetlana G. VorsanovaY. B. YurovL. Z. Kazantzeva Original Investigations Pages: 173 - 174
Intrinsic potential for high fetal hemoglobin production in a Druze family with β-thalassemia is due to an unlinked genetic determinant Ariella OppenheimAvi YaariBarbara Miller Original Investigations Pages: 175 - 180
Analysis of gene-dosage effects on the expression of CD18 by trisomy 21 lymphoblastoid cell-lines using a statistical model to fit flow cytometry profiles W. G. BardsleyB. P. McMurrayG. M. Taylor Original Investigations Pages: 181 - 186
Assignment of the gene for central core disease to chromosome 19 Eric A. HaanC. Jane FreemantleJohn C. Mulley Original Investigations Pages: 187 - 190
Multiple levels of analysis of an IGHG4 gene deletion Andrea BottaroUmberto CariotaAngelo O. Carbonara Original Investigations Pages: 191 - 197
Changing paternal age distribution and the human mutation rate in Europe Bernadette ModellAnver Kuliev Original Investigations Pages: 198 - 202
Hereditary retinoblastoma: can balanced insertion entirely explain the differences of expressivity among families? Catherine Bonaïti-PelliéFrançoise Clerget-DarpouxMarie-Claude Babron Original Investigations Pages: 203 - 208
Association analysis of lipid levels and apolipoprotein restriction fragment length polymorphisms Ola MyklebostSissel RogneHans Prydz Original Investigations Pages: 209 - 214
Heterozygous expression of X-linked chondrodysplasia punctata Doris WöhrleGotthold BarbiPeter Steinbach Original Investigations Pages: 215 - 218
The molecular genetic analysis of haemophilia A; characterization of six partial deletions in the factor VIII gene D. S. MillarR. A. SteinbrecherD. N. Cooper Original Investigations Pages: 219 - 227
A recombination map of the human X-chromosome R. G. Del MastroP. A. FarndonMichael W. Kilpatrick Original Investigations Pages: 228 - 230
Abnormal hemoglobins in the Silk Road region of China Hou-jun LiXian-ning ZhaoTitus H. J. Huisman Original Investigations Pages: 231 - 235
The major cystic fibrosis mutation in a British population C. J. McMahonS. A. GenetS. Malcolm Original Investigations Pages: 236 - 237
The gene coding for the α-chain of human propionyl-CoA carboxylase maps to chromosome band 13q32 I. KennerknechtT. SuormalaE. R. Baumgartner Short Communications Pages: 238 - 240
Germinal mosaicism from grand-paternal origin in a family with Duchenne muscular dystrophy Mireille ClaustresPaule KjellbergJacques Demaille Short Communications Pages: 241 - 243
BglII restriction fragment length polymorphisms at the human p53 gene locus Umesh MasharaniDavid Wolf OriginalPaper Pages: 244 - 244