Deletion of the long arm of chromosome 8 resulting from a de novo translocation t(4;8) (q13;q213) B. DallapiccolaL. SantoroE. Gandini Original Investigations Pages: 125 - 130
Mosaic trisomy 9: Two additional cases Marleen R. TroppMarie Currie Original Investigations Pages: 131 - 135
Monosomy 21 in a human spontaneous abortus A. M. KulievK. N. GrinbergE. A. Bogomazov Original Investigations Pages: 137 - 145
Unusually long survival in a case of full triploidy of maternal origin J. P. FrynsA. van de KerckhoveH. van den Berghe Original Investigations Pages: 147 - 155
Hirschsprung's disease and congenital deafness Arthur G. WeinbergGuido CurrarinoAbraham M. Besserman Original Investigations Pages: 157 - 161
Inbreeding in recessive diseases Paul TchenEtienne BoisJosselyne Kaplan Original Investigations Pages: 163 - 167
Genetic considerations on association between HLA and disease L. E. Nijenhuis Original Investigations Pages: 175 - 182
Inheritance of Ag-stainability of nucleolus organizer regions A. -V. MikelsaarH. G. SchwarzacherP. Wagenbichler Original Investigations Pages: 183 - 188
Length of human constitutive heterochromatin in relation to chromosomal contraction Petr BalíčekJan ŽižkaHana Skalská Original Investigations Pages: 189 - 193
Psoralen/UVA treatment and chromosomes Helga WaksvikAnton BrøggerJon Stene Original Investigations Pages: 195 - 207
Electrophoretic and kinetic studies of human erythrocytes deficient in pyrimidine 5′-nucleotidase Raymonde RosaHenri RochantJean Rosa Original Investigations Pages: 209 - 215
Linkage between phosphoglycerate kinase and Xg in a large German kindred Andreas J. SchwabWolfgang K. G. Krietsch Original Investigations Pages: 217 - 221
Glyoxalase I polymorphism in South African Bantu-speaking Negroids K. BenderRosita FrankH. W. Hitzeroth Original Investigations Pages: 223 - 226
No evidence for linkage disequilibrium between Bf and GLO in African Negroids K. BenderG. MauffH. W. Hitzeroth Original Investigations Pages: 227 - 230
Size variation polymorphisms of the short arm of human acrocentric chromosomes determined by R-banding by fluorescence using acridine orange (RFA) Ram S. VermaHarvey DosikHerbert A. Lubs Short Communications Pages: 231 - 234
A rare adenosine deaminase allele (ADA6) in an Arab Moslem village in Israel Sarah Nevo Short Communications Pages: 235 - 238
Two cases of trisomy 21 and one XXY case with atypical clinical features Anne HobbsMarina SeabrightSarah Mould Clinical Case Reports Pages: 239 - 244
Partial 9q trisomy associated with a 9,21 translocation Yves ChamlaCatherine BilbeissiJacques Battin Clinical Case Reports Pages: 245 - 248
De novo trisomy 9pter→q13 Nataline B. KardonHelen R. SalwenEdmund C. Jenkins Addendum Pages: 249 - 249