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Human Genetics|October 9, 2013
A hemizygous GYG2 mutation and Leigh syndrome: a possible link?Eri Imagawa, Hitoshi Osaka, Akio Yamashita, et al.Human Genetics|October 9, 2013
No evidence of interaction between known lipid-associated genetic variants and smoking in the multi-ethnic PAGE populationLogan Dumitrescu, Cara L Carty, Nora Franceschini, et al.Human Genetics|October 15, 2013
Network.assisted analysis to prioritize GWAS results: principles, methods and perspectivesPeilin Jia, Zhongming ZhaoHuman Genetics|October 12, 2013
A genome-wide association study of severe teenage acne in European AmericansMingfeng Zhang, Abrar A Qureshi, David J Hunter, et al.Human Genetics|January 1, 1985
Variant of ataxia-telangiectasia with low-level radiosensitivityM Fiorilli, A Antonelli, G Russo, et al.Human Genetics|October 10, 2013
Cancer genomics identifies disrupted epigenetic genesLaia Simó-Riudalbas, Manel EstellerHuman Genetics|May 10, 2012
Reduced interferon (IFN)-α conditioned by IFNA2 (-173) and IFNA8 (-884) haplotypes is associated with enhanced susceptibility to severe malarial anemia and longitudinal all-cause mortalityPrakasha Kempaiah, Samuel B Anyona, Evans Raballah, et al.Human Genetics|May 31, 2012
Evaluation of PRDM9 variation as a risk factor for recurrent genomic disorders and chromosomal non-disjunctionChristelle Borel, Fanny Cheung, Helen Stewart, et al.Human Genetics|September 1, 1994
Characterization of the three genotypes of low Km aldehyde dehydrogenase in a Japanese populationT Takeshita, K Morimoto, X Mao, et al.Pageof 957