Human Genome Epidemiology Literature Finder
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Query Trace: Craniofacial Abnormalities and CYP2C9[original query] |
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Maternal EPHX1 polymorphisms and risk of phenytoin-induced congenital malformations. Pharmacogenetics and genomics 2010 Jan 20 (1): 58-63. Azzato Elizabeth M, Chen Renee A, Wacholder Sholom, Chanock Stephen J, Klebanoff Mark A, Caporaso Neil |
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