Structure and variability of human chromosomes analyzed by recent techniques W. Schnedl Review Articles Pages: 1 - 9
Trisomy 10p due to t(5;10)(p15;p11) segregating in a large sibship Elke BackW. VogelL. Schuchmann Original Investigations Pages: 11 - 17
Patterns of association in the human metaphase complement: Ring analysis and estimation of associativity of specific chromosome regions Toby C. RodmanBetty J. FlehingerRichard D. Squire Original Investigations Pages: 19 - 34
Identification of the origin of triploidy by HLA markers P. CouillinJ. HorsA. Boué Original Investigations Pages: 35 - 44
Reduced frequencies of Mitomycin-C induced sister chromatid exchanges in AKR Mice David KramEdward L. Schneider Original Investigations Pages: 45 - 51
Analysis of the Gc polymorphism in human populations by isoelectrofocusing on polyacrylamide gels. Demonstration of subtypes of the Gc1 allele and of additional Gc variants J. ConstansM. ViauM. J. Palisson Original Investigations Pages: 53 - 60
Human erythrocyte pyruvate kinase deficiency: The use of a kinetic study of mutant enzymes for the detection of heterozygotes E. D. SprengersJ. MarieG. E. J. Staal Original Investigations Pages: 61 - 72
HLA antigen, gene, and haplotype frequencies in Thailand J. GreinerE. SchleiermacherF. Vogel Original Investigations Pages: 73 - 87
An increased frequency of chromosomal changes and SCE's in cultured blood lymphocytes of 12 subjects vaccinated against smallpox Sakari KnuutilaJorma Mäki-PaakkanenEeva Hokkanen Short Communications Pages: 89 - 96
Occurrence of 1st division metaphases in human lymphocyte cultures Peter E. CrossenWilliam F. Morgan Short Communications Pages: 97 - 100
Balanced t(8;9)(q12;q33)pat carrier with phenotypic abnormalities attributable to a de novo terminal deletion of the long arm of chromosome 7 Brian BiedermanPeter Bowen Clinical Case Reports Pages: 101 - 107
Variant chromosome 3 (inv3) in normal newborns and their parents, and in children with mental retardation A. -V. MikelsaarTiiu IlusSirje Kivi Clinical Case Reports Pages: 109 - 113
Terminal deletion of (1)(q42) and its phenotypical manifestations Milly AndrleA. ErlachA. Rett Clinical Case Reports Pages: 115 - 120