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Biochemical and Molecular Medicine|April 1, 1995
Frequency of a specific cytochrome P4502D6B (CYP2D6B) mutant allele in clinically differentiated groups of patients with Parkinson diseaseS N Akhmedova, E A Pushnova, A F Yakimovsky, et al.
Molecular Genetics and Metabolism|February 3, 2000
Gene-gene interaction in the RAS system in the predisposition to myocardial infarction in elder population of St. Petersburg (Russia)E V Fomicheva, S P Gukova, V I Larionova-Vasina, et al.
Biochemical and Molecular Medicine|August 1, 1996
CYP2D6 genotyping in a Russian population using a novel approach for identification of the CYP2D6A mutationS N Akhmedova, E A Pushnova, S Anisimov, et al.
Diabetes|November 14, 1997
The effect of HLA-B allele on the IDDM risk defined by DRB1*04 subtypes and DQB1*0302S Nejentsev, H Reijonen, B Adojaan, et al.
European Journal of Human Genetics : EJHG|January 1, 1995
Complete spectrum of PAH mutations in Tataria: presence of Slavic, Turkic and Scandinavian mutationsA I Kuzmin, R C Eisensmith, A A Goltsov, et al.
The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences|February 24, 2001
Age-associated accumulation of the apolipoprotein C-III gene T-455C polymorphism C allele in a Russian populationS V Anisimov, M V Volkova, L V Lenskaya, et al.
Biochemical Medicine and Metabolic Biology|April 1, 1994
Identification of the linkage of mutations causing cystic fibrosis to different alleles of a tetranucleotide repeat in intron 6a of the CFTR genePotapova OYu, O V Voronina, V S Gaitskhoki, et al.
Biochemical Medicine and Metabolic Biology|October 1, 1993
Linkage disequilibrium between cystic fibrosis mutations and polymorphic 4-bp repeat within CFTR geneV S Gaitskhoki, O V Voronina, Potapova OYu, et al.
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