Omphalocele and partial trisomy 1q syndrome H. ChenJ. J. GershanikI. D. Sanusi Original Investigations Pages: 1 - 4
Chromosomes in acute leukemia E. L. PrigoginaE. W. FleischmanI. S. Peterson Original Investigations Pages: 5 - 16
Segregation of rat chromosomes in somatic cell hybrids between rat cells and HT 1080 human fibrosarcoma cells G. G. D'AnconaC. M. Croce Original Investigations Pages: 17 - 21
Heritable fragile sites on human chromosomes G. R. SutherlandP. Leonard Original Investigations Pages: 29 - 30
Genetic studies of complement C4 in man G. B. PetersenInger Juncker SørensenL. U. Lamm Original Investigations Pages: 31 - 36
Hurler-Scheie phenotype: A report of two pairs of inbred sibs N. KaibaraM. EguchiK. Takagishi Original Investigations Pages: 37 - 41
Characterization of some erythrocyte G6PD variants by isoelectric focusing H. VergnesH. Brun Original Investigations Pages: 43 - 45
Assignment of a gene for human quinoid-dihydropteridine reductase (QDPR, EC 1.6.5.1) to chromosome 4 P. KuhlK. OlekK. -H. Grzeschik Original Investigations Pages: 47 - 49
H-Y antigen in Swyer syndrome and the genetics of XY gonadal dysgenesis C. A. Moreira-FilhoS. P. A. ToledoA. Wajntal Original Investigations Pages: 51 - 56
H-Y antigen-positive male pseudohermaphroditism with 45,X/46,XYq-mosaicism J. B. MaihesD. E. PittawayW. D. Grafton Original Investigations Pages: 57 - 63
Qualitative and quantitative study of the growth and cell surface properties of Huntington's disease fibroblasts and age-matched controls J. J. CassimanJ. VerlindenH. Van den Berghe Original Investigations Pages: 75 - 86
Human alcohol dehydrogenase ADH2 and ADH3 polymorphisms in ethnic Chinese and Indians of West Malaysia Y. -S. TengS. JehanL. E. Lie-Injo Original Investigations Pages: 87 - 90
Characterization of alpha-1-antitrypsin by isoelectric focusing on an ultrathin polyacrylamide gel layer G. MassiA. FabianoP. Auconi Original Investigations Pages: 91 - 95
Improved screening test for abnormal hemoglobins from dried blood samples K. AltlandM. KaempferH. Granda Original Investigations Pages: 97 - 100
Gm allotypes and racial admixture in two Brazilian populations H. SchneiderF. M. Salzano Original Investigations Pages: 101 - 105
Demonstration of Y/autosomal translocations using distamycin A M. Schmid Short Communications Pages: 107 - 109
A new translocation in Burkitt's tumor cells R. BergerA. BernheimN. Colbert Short Communications Pages: 111 - 112
Failure to demonstrate abnormal lymphocyte capping in humans, mice and hamsters with muscular dystrophy M. E. GershwinR. G. TaylorBarbara Finlayson Short Communications Pages: 113 - 114
Deficiency of arylsulfatase C in cultured skin fibroblasts of X-linked ichthyosis J. Ch. MeyerH. WeissU. W. Schnyder Short Communications Pages: 115 - 116
Pericentric inversion in chromosome No.2 as a de novo mutation Ulla HesselbjergUrsula Friedrich Clinical Case Reports Pages: 117 - 119
Partial trisomy 7q and probable partial monosomy of 5p in the son of a mother with a reciprocal translocation between 5p and 7q A. SchinzelO. Tönz Clinical Case Reports Pages: 121 - 124
Familial transmission of a translocation Y/14 C. H. C. M. BuysG. J. P. A. AndersA. Y. van der Hoek-van der Veen Clinical Case Reports Pages: 125 - 127
Exclusion of the localization of the Gm, Pi, and C3 genes on 6q25→6qter through blood group analysis of the patients of Schmid, D'Apuzzo and rossi (Hum. Genet. 46, 279–284, 1979) K. BenderK. BurckhardtK. Schroetter Letters to the Editors Pages: 129 - 130