Variable substructure in the secondary constriction of the human chromosome 1 J. SigmundS. Schwarz Original Investigations Pages: 1 - 4
A homozygote for a serum albumin variant of the fast type G. VanzettiF. PortaM. Fraccaro Original Investigations Pages: 5 - 9
A two-year-old patient with an atypical expression of GM1-β-galactosidase deficiency: Biochemical, immunological, and cell genetic studies A. J. J. ReuserG. AndriaD. Halley Original Investigations Pages: 11 - 19
Langer type of mesomelic dwarfism as the possible homozygous expression of dyschondrosteosis J. P. FrynsH. Van Den Berghe Original Investigations Pages: 21 - 27
Partial trisomy 10q Johanna M. Klep-de PaterJan B. BijlsmaJan O. van Hemel Original Investigations Pages: 29 - 40
Biochemical characteristics of Ehlers-Danlos syndrome type VI in a family with one affected infant T. KriegUrsula FeldmannP. K. Müller Original Investigations Pages: 41 - 49
Effects of various cyclophosphamide concentrations in vivo on sister chromatid exchanges (SCE) and chromosome aberrations of Chinese hamster bone marrow cells G. Roszinsky-KöcherG. Röhrborn Original Investigations Pages: 51 - 55
Sister chromatid exchanges and aging Edward L. SchneiderBrian Gilman Original Investigations Pages: 57 - 63
Serum zinc levels in heterozygous carriers of the gene for acrodermatitis enteropathica P. Ølholm-Larsen Original Investigations Pages: 65 - 74
Cytological analyses of a 14p+variant by means of N-banding and combinations of silver staining and chromosome bandings Y. F. LauW. WerteleckiF. E. Arrighi Original Investigations Pages: 75 - 82
Isoelectric focusing of rare transferrin (Tf) variants and common TfC subtypes P. KühnlW. SpielmannW. Weber Original Investigations Pages: 83 - 87
Isoelectrofocusing of erythrocyte galactose 1 phospho uridyl transferase in a family with both galactosemia and duarte variants F. SchapiraC. GregoriC. Vigneron Original Investigations Pages: 89 - 96
PTC-Tasting ability in populations living in Kirghizia with special reference to hypersensitivity: Its relation to sex and age A. AbraimovM. M. Mirrakhimov Original Investigations Pages: 97 - 105
Origin of the extra chromosome in trisomy 21 J. F. MatteiM. G. MatteiF. Giraud Short Communications Pages: 107 - 110
Partial monosomy of the long arm of chromosome 16: A distinct clinical entity? J. P. FrynsJ. Bande-KnopsH. Van Den Berghe Clinical Case Reports Pages: 115 - 120