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Journal of Human Genetics|November 30, 2005
Evaluation of a methylenetetrahydrofolate-dehydrogenase 1958G>A polymorphism for neural tube defect riskPatrizia De Marco, Elisa Merello, Maria Grazia Calevo, et al.Journal of Human Genetics|October 28, 2005
Analysis of the NSD1 promoter region in patients with a Sotos syndrome phenotypeRemco Visser, Tomonobu Hasegawa, Norio Niikawa, et al.Journal of Human Genetics|October 18, 2005
Possible risk modification by CYP1A1, GSTM1 and GSTT1 gene polymorphisms in lung cancer susceptibility in a South Indian populationLeelakumari Sreeja, Vani Syamala, Sreedharan Hariharan, et al.Journal of Human Genetics|November 14, 2009
Evidence for a founder mutation causing DFNA5 hearing loss in East AsiansHong-Joon Park, Hyun-Ju Cho, Jeong-In Baek, et al.Journal of Human Genetics|December 5, 2009
Replication of a genome-wide association study of panic disorder in a Japanese populationTakeshi Otowa, Hisashi Tanii, Nagisa Sugaya, et al.Journal of Human Genetics|November 21, 2009
Association between ESR1 and ESR2 gene polymorphisms and hyperlipidemia in Chinese Han postmenopausal womenTeng Zhao, Di Zhang, Yun Liu, et al.Journal of Human Genetics|November 21, 2009
Examination of FMR1 transcript and protein levels among 74 premutation carriersEmmanuel Peprah, Weiya He, Emily Allen, et al.Journal of Human Genetics|January 30, 2010
Novel mutations in the SIL1 gene in a Japanese pedigree with the Marinesco-Sjögren syndromeTaichi Takahata, Koki Yamada, Yoshihisa Yamada, et al.Journal of Human Genetics|March 20, 1999
A Gln/Arg polymorphism at codon 349 of the hBUBR1 geneT Katagiri, M Futamura, Y NakamuraJournal of Human Genetics|March 20, 1999
Isolation and mapping of a polymorphic CA repeat sequence at the human VRK1 locusJ Sugimoto, T Yamauchi, T Hatakeyama, et al.Pageof 352