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Journal of Human Genetics|May 12, 2007
Mutations in the WFS1 gene are a frequent cause of autosomal dominant nonsyndromic low-frequency hearing loss in JapaneseHisakuni Fukuoka, Yukihiko Kanda, Shuji Ohta, et al.Journal of Human Genetics|August 1, 2009
Structural bases of GM1 gangliosidosis and Morquio B diseaseMizuki Morita, Seiji Saito, Kazuyoshi Ikeda, et al.Journal of Human Genetics|July 25, 2009
Mutations in mitochondrial DNA polymerase-gamma promote breast tumorigenesisKeshav K Singh, Vanniarajan Ayyasamy, Kjerstin M Owens, et al.Journal of Human Genetics|August 29, 2009
Impact of ACE and ApoE polymorphisms on myocardial perfusion: correlation with myocardial single photon emission computed tomographic imagingPanagiotis Georgoulias, Greta Wozniak, Maria Samara, et al.Journal of Human Genetics|August 22, 2009
Single nucleotide polymorphism in ABCG2 is associated with irinotecan-induced severe myelosuppressionPei-Chieng Cha, Taisei Mushiroda, Hitoshi Zembutsu, et al.Journal of Human Genetics|August 22, 2009
Central areolar choroidal dystrophy associated with inherited drusen in a multigeneration Tunisian family: exclusion of the PRPH2 gene and the 17p13 locusFarah Ouechtati, Olfa Belhadj Tahar, Amin Mhenni, et al.Journal of Human Genetics|August 13, 2010
Polymorphisms in NRXN3, TFAP2B, MSRA, LYPLAL1, FTO and MC4R and their effect on visceral fat area in the Japanese populationKikuko Hotta, Michihiro Nakamura, Takahiro Nakamura, et al.Journal of Human Genetics|April 17, 2010
Different effects of apolipoprotein A5 SNPs and haplotypes on triglyceride concentration in three ethnic originsGie Ken-Dror, Uri Goldbourt, Rachel DanknerJournal of Human Genetics|June 25, 2010
Examination of disease-based selection, demographic history and population structure in European Y-chromosome haplogroup IEfe Sezgin, Alyssa Drosdak, Carl McIntosh, et al.Journal of Human Genetics|June 3, 2011
Maternal age effect on the development of Prader-Willi syndrome resulting from upd(15)mat through meiosis 1 errorsKeiko Matsubara, Nobuyuki Murakami, Toshiro Nagai, et al.Pageof 352