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Journal of Human Genetics|April 2, 2002
Mutational and haplotype analysis of AGL in patients with glycogen storage disease type IIIAsako Horinishi, Minoru Okubo, Nelson L S Tang, et al.
Journal of Human Genetics|December 21, 2005
ALDH2 and CYP2E1 genotypes, urinary acetaldehyde excretion and the health consequences in moderate alcohol consumersYuichi Yamada, Tsunehiko Imai, Masao Ishizaki, et al.
Journal of Human Genetics|December 24, 2005
The CAG repeat at the Huntington disease gene in the Portuguese population: insights into its dynamics and to the origin of the mutationMaria do Carmo Costa, Paula Magalhães, Laura Guimarães, et al.
Journal of Human Genetics|December 24, 2005
Association study of semaphorin 7a (sema7a) polymorphisms with bone mineral density and fracture risk in postmenopausal Korean womenJung-Min Koh, Bermseok Oh, Jong Yong Lee, et al.
Journal of Human Genetics|November 18, 2005
Association of CD14 promoter polymorphisms and soluble CD14 levels in mite allergen sensitization of children in TaiwanChoon-Yee Tan, Yi-Lin Chen, Lawrence Shih-Hsin Wu, et al.
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.
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