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Journal of Human Genetics|June 14, 2006
Inflammation as a risk factor for myocardial infarctionToshihiro Tanaka, Kouichi OzakiJournal of Human Genetics|March 28, 2002
Functional polymorphism in the promoter region of the gelatinase B gene in relation to coronary artery disease and restenosis after percutaneous coronary interventionHyun-Jai Cho, In-Ho Chae, Kyung-Woo Park, et al.Journal of Human Genetics|April 13, 2002
Anthropological implication of the SDF1-3'A allele distribution in Southeast Asia and MelanesiaRyosuke Kimura, Augustinus Soemantri, Wannapa Settheetham-Ishida, et al.Journal of Human Genetics|November 14, 2009
A novel complex mutation in MSH2 contributes to both Muir-Torre and Lynch SyndromeSheron Perera, Lily Ramyar, Angie Mitri, et al.Journal of Human Genetics|November 14, 2009
Identification of novel L2HGDH gene mutations and update of the pathological spectrumLaura Vilarinho, Sandra Tafulo, Michelina Sibilio, et al.Journal of Human Genetics|November 14, 2009
The key role of patrilineal inheritance in shaping the genetic variation of Dagestan highlandersLaura Caciagli, Kazima Bulayeva, Oleg Bulayev, et al.Journal of Human Genetics|November 7, 2009
No influence of FAT polymorphisms in response to aripiprazoleChi-Un Pae, Alberto Chiesa, Laura Mandelli, et al.Journal of Human Genetics|November 7, 2009
Mutant alleles associated with late-onset ornithine transcarbamylase deficiency in male patients have recurrently arisen and have been retained in some populationsSanae Numata, Yoshiro Koda, Kenji Ihara, et al.Journal of Human Genetics|November 3, 2009
Common genetic variants in pre-microRNAs are associated with risk of coal workers' pneumoconiosisMeilin Wang, Yang Ye, Haiyang Qian, et al.Journal of Human Genetics|June 2, 2025
Novel susceptibility gene SLC23A2 functions via PI3K-AKT-mTOR pathway in etiology of non-syndromic cleft palateBin Yin, Mu-Jia Li, Jia-Lin Sun, et al.Pageof 351