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Human Heredity|May 9, 2000
A new inherited interstitial deletion of the distal long arm of chromosome 4S M Aladhami, C P Gould, F A MuhammadHuman Heredity|July 19, 2000
A sib-pair regression model of linkage disequilibrium for quantitative traitsL R CardonHuman Heredity|July 19, 2000
The human HNF-3 genes: cloning, partial sequence and mutation screening in patients with impaired glucose homeostasisM A Navas, C Vaisse, S Boger, et al.Human Heredity|June 12, 1999
Detection of the most common G6PD gene mutations in Chinese using amplification refractory mutation systemC S Du, X Ren, L Chen, et al.Human Heredity|June 12, 1999
Simple tandem repeat polymorphisms in the neuronal nitric oxide synthase gene in different ethnic populationsH Grasemann, J M Drazen, A Deykin, et al.Human Heredity|June 12, 1999
Familiality of quantitative metabolic traits in Finnish families with non-insulin-dependent diabetes mellitus. Finland-United States Investigation of NIDDM Genetics (FUSION) Study investigatorsR M Watanabe, T Valle, E R Hauser, et al.Human Heredity|June 12, 1999
Mutation analysis in patients with congenital adrenal hyperplasia in the Spanish population: identification of putative novel steroid 21-hydroxylase deficiency alleles associated with the classic form of the diseaseM N Lobato, M L Ordóñez-Sánchez, M T Tusié-Luna, et al.Human Heredity|June 12, 1999
Gln --> Arg 191 polymorphism of paraoxonase and Parkinson's diseaseS Akhmedova, S Anisimov, A Yakimovsky, et al.Human Heredity|January 1, 1976
Heterogenous glycogen storage disease in one familyN Domaniç, N Akman, P Ozand, et al.Human Heredity|August 7, 1999
The analysis of parental origin of alleles may detect susceptibility loci for complex disordersA D Paterson, D M Naimark, A PetronisPageof 237