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Human Heredity|January 1, 1984
DNA polymorphism of the RC8 sequence on the short arm of the X chromosome in a French populationC Rahuel, K Y Ngo, J P Cartron, et al.Human Heredity|March 1, 1995
Ethnic differences in allele frequencies of two microsatellite markers closely linked to the locus for polycystic kidney disease 1 (PKD1)H Wang, S Kuwata, T Juji, et al.Human Heredity|January 1, 1984
Aldehyde dehydrogenase isozyme deficiency and alcohol sensitivity in four different Chinese populationsH W Goedde, H G Benkmann, L Kriese, et al.Human Heredity|December 15, 2005
Haplotype association analysis of AGT variants with hypertension-related traits: the HyperGEN studyC Charles Gu, Yen-Pei C Chang, Steven C Hunt, et al.Human Heredity|January 1, 1981
Isoelectric focusing of human red cell phosphoglucomutase (PGM1): phenotype distribution in the Swiss population - rare phenotypesR Scherz, R Pflugshaupt, R BütlerHuman Heredity|January 1, 1976
Blood and serum protein groups of the dama of South-West AfricaR Knussmann, R KnussmannHuman Heredity|January 1, 1978
Sequence of action of genes at the secretor, H, ABO and Lewis lociB BoettcherHuman Heredity|January 1, 1981
Dermatoglyphic studies in the parents of trisomy 21 children I. Distribution of dermatoglyphic discriminantsD LoeschHuman Heredity|March 1, 1994
Molecular characterisation of red cell glucose-6-phosphate dehydrogenase deficiency in north-west PakistanN Saha, M Ramzan, J S Tay, et al.Human Heredity|March 1, 1994
Report of three cases of mucopolysacchaidoses and an unusual case of hyperaminoaciduria detected during the screening of mentally retarded childrenK S Devi, P Veeraju, B S RaoPageof 237