Chromosomal in situ suppression hybridization of human gonosomes and autosomes and its use in clinical cytogenetics A. JauchC. DaumerT. Cremer Original Investigations Pages: 145 - 150
Identification of sequences of chromosome 7 that are expressed in sweat gland epithelial cells Julie BurnsGeorg MelmerManuel Buchwald Original Investigations Pages: 151 - 156
Linkage disequilibrium between DNA polymorphisms within the porphobilinogen deaminase gene G. A. ScobieA. J. UrquhartP. R. Harrison Original Investigations Pages: 157 - 159
RFLP analysis of three different types of acute intermittent porphyria R. KauppinenL. PeltonenP. Mustajoki Original Investigations Pages: 160 - 164
Epidemiological and linkage studies on Huntington's disease in Italy Marina FrontaliPatrizia MalaspinaAndrea Novelletto Original Investigations Pages: 165 - 170
Chromosomal localization of the human protamine genes, PRM1 and PRM2, to 16p13.3 by in situ hybridization Franck ViguiéLionel DomenjoudPhilippe Chevaillier Original Investigations Pages: 171 - 174
The similarity of phenotypic effects caused by Xp and Xq deletions in the human female: a hypothesis Eeva ThermanBarbara Susman Original Investigations Pages: 175 - 183
Centromere splitting in bladder cancer Georgina BerrozpeMaria Rosa CaballinJosé Egozcue Original Investigations Pages: 184 - 186
Heterogeneities in the distribution of (GACA)n simple repeats in the karyotypes of primates and mouse Indrajit NandaClaudia DeubelbeissMichael Schmid Original Investigations Pages: 187 - 194
Lecithin cholesterol acyl transferase deficiency: molecular analysis of a mutated allele Roberto TaramelliMarco PontoglioJohn McLean Original Investigations Pages: 195 - 199
Two factor IX mutations in the family of an isolated haemophilia B patient: direct carrier diagnosis by amplification mismatch detection (AMD) A. J. MontandonP. M. GreenF. Giannelli Original Investigations Pages: 200 - 204
Deletion mapping of 39 random isolated Y-chromosome DNA fragments C. J. J. OosthuizenJ. S. HerbertA. E. Retief Original Investigations Pages: 205 - 210
Population data on acute infantile and chronic childhood spinal muscular atrophy in Warsaw Aribert W. J. SpieglerIrena Hausmanowa-PetrusewiczAnna Kłopocka Original Investigations Pages: 211 - 214
Analysis of 7 polymorphic markers at chromosome 11q22-23 in 35 ataxia telangiectasia families; further evidence of linkage C. M. McConvilleC. G. WoodsA. M. R. Taylor Original Investigations Pages: 215 - 220
Linkage study of a large family with autosomal dominant polycystic kidney disease with reduced expression Lucien BachnerMarie Claude VinetJean-Claude Kaplan Original Investigations Pages: 221 - 227
Family studies of hereditary hemochromatosis in Denmark and the Faroe Islands Nils MilmanNiels GraudalKirsten Fenger Original Investigations Pages: 228 - 232
Linkage of aspartylglucosaminuria (AGU) to marker loci on the long arm of chromosome 4 Kristiina GrönPertti AulaLeena Peltonen Original Investigations Pages: 233 - 236
Human αB-crystallin (CRYA2) gene mapped to chromosome 11q12-q23 Ruud H. BrakenhoffAd H. M. Geurts van KesselJohn G. G. Schoenmakers Original Investigations Pages: 237 - 240
Improved fragile site detection with trimethoprim Doris A. McLeanMichael J. W. Faed Short Communications Pages: 241 - 243
Centromeric heterochromatin instability of chromosomes 1, 9, and 16 in variable immunodeficiency syndrome — a virus-induced phenomenon? Oskar A. Haas Short Communications Pages: 244 - 246
An interstitial deletion in Xp22.3 in a family with X-linked recessive chondrodysplasia punctata and short stature Christine PetitJudith MelkiPierre Maroteaux Short Communications Pages: 247 - 250
DNA polymorphism of the human complement component C7 gene in familial deficiencies Eliecer CotoEduardo Martínez-NavesCarlos López-Larrea Short Communications Pages: 251 - 252
Homologous Robertsonian translocation (21q21q) and abortions T. SudhaP. M. Gopinath Clinical Case Report Pages: 253 - 255
