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Journal of Human Genetics|June 6, 2014
No association between typical European mitochondrial variation and prostate cancer risk in a Spanish cohortLaura Fachal, Antonio Gómez-Caamaño, Vanesa Alvarez Iglesias, et al.Journal of Human Genetics|September 7, 2012
Functional analysis of a lung cancer risk haplotype in the IL1B gene regulatory regionNina E Landvik, Kent Hart, Aage Haugen, et al.Journal of Human Genetics|September 21, 2012
Pentanucleotide repeat-primed PCR for genetic diagnosis of spinocerebellar ataxia type 31Takayuki Ishige, Setsu Sawai, Sakae Itoga, et al.Journal of Human Genetics|September 21, 2012
Is the prevalence of MTHFR C677T polymorphism associated with ultraviolet radiation in Eurasia?Wang Yafei, Pei Lijun, Wang Jinfeng, et al.Journal of Human Genetics|September 14, 2012
Huntington disease-like 2 (HDL2) in Venezuela: frequency and ethnic originIrene Paradisi, Vassiliki Ikonomu, Sergio AriasJournal of Human Genetics|September 25, 1998
Joint laxity, vitreoretinal degeneration, facial abnormalities, and generalized skeletal alterations: a new syndrome?G Nishimura, T Hasegawa, K Sugii, et al.Journal of Human Genetics|September 25, 1998
Novel MEN1 gene mutations in familial multiple endocrine neoplasia type 1A Sakurai, S Shirahama, M Fujimori, et al.Journal of Human Genetics|August 24, 2012
Association of IREB2 and CHRNA3/5 polymorphisms with COPD and COPD-related phenotypes in a Chinese Han populationHaixia Zhou, Jing Yang, Dengxue Li, et al.Journal of Human Genetics|August 24, 2012
Genotype-based association analysis via entropyYu-Mei Li, Yang XiangJournal of Human Genetics|August 24, 2012
Confirmation and refinement of an autosomal dominant congenital motor nystagmus locus in chromosome 1q31.3-q32.1Lin Li, Xueshan Xiao, Changxian Yi, et al.Pageof 351