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Journal of Human Genetics|February 18, 2011
Mitochondrial DNA and Y-chromosomal stratification in Iran: relationship between Iran and the Arabian PeninsulaMaria C Terreros, Diane J Rowold, Sheyla Mirabal, et al.Journal of Human Genetics|February 18, 2011
Hypospadias associated with hypertelorism, the mildest phenotype of Opitz syndromeXufeng Zhang, Yougen Chen, Shentiang Zhao, et al.Journal of Human Genetics|March 27, 2010
Genetic structures of the Tibetans and the Deng people in the Himalayas viewed from autosomal STRsLongli Kang, Shilin Li, Sameer Gupta, et al.Journal of Human Genetics|June 25, 2010
The GCKR rs780094 polymorphism is associated with susceptibility of type 2 diabetes, reduced fasting plasma glucose levels, increased triglycerides levels and lower HOMA-IR in Japanese populationHiroshi Onuma, Yasuharu Tabara, Ryuichi Kawamoto, et al.Journal of Human Genetics|July 16, 2010
A novel GATA6 mutation in patients with tetralogy of Fallot or atrial septal defectXiaoping Lin, Zhaoxia Huo, Xingyuan Liu, et al.Journal of Human Genetics|July 3, 2010
Hair roots as an mRNA source for mutation analysis of Usher syndrome-causing genesHiroshi Nakanishi, Masafumi Ohtsubo, Satoshi Iwasaki, et al.Journal of Human Genetics|August 13, 2010
Human endogenous retrovirus K14C drove genomic diversification of the Y chromosome during primate evolutionHo-Su Sin, Eitetsu Koh, Dae-Soo Kim, et al.Journal of Human Genetics|July 29, 2010
Association of the leptin gene with knee osteoarthritis susceptibility in a Han Chinese population: a case-control studyJianghui Qin, Dongquan Shi, Jin Dai, et al.Journal of Human Genetics|August 20, 2010
A novel homozygous MMP2 mutation in a patient with Torg-Winchester syndromeSeon-Yong Jeong, Bo-Young Kim, Hyon J Kim, et al.Journal of Human Genetics|June 4, 2010
Phenotypic variability in a family with Townes-Brocks syndromeYosuke Sudo, Chikahiko Numakura, Akiko Abe, et al.Pageof 351