Association between maternal single nucleotide polymorphisms in genes regulating glucose metabolism and risk for neural tube defects in offspring.

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Title: Association between maternal single nucleotide polymorphisms in genes regulating glucose metabolism and risk for neural tube defects in offspring.
Authors: Fu Y; Institute of Reproductive and Child Health / Ministry of Health Key Laboratory of Reproductive Health, School of Public Health, Peking University, Beijing, China., Wang LL; Institute of Reproductive and Child Health / Ministry of Health Key Laboratory of Reproductive Health, School of Public Health, Peking University, Beijing, China., Yi D; Institute of Reproductive and Child Health / Ministry of Health Key Laboratory of Reproductive Health, School of Public Health, Peking University, Beijing, China., Jin L; Institute of Reproductive and Child Health / Ministry of Health Key Laboratory of Reproductive Health, School of Public Health, Peking University, Beijing, China., Liu J; Institute of Reproductive and Child Health / Ministry of Health Key Laboratory of Reproductive Health, School of Public Health, Peking University, Beijing, China., Zhang Y; Institute of Reproductive and Child Health / Ministry of Health Key Laboratory of Reproductive Health, School of Public Health, Peking University, Beijing, China., Ren A; Institute of Reproductive and Child Health / Ministry of Health Key Laboratory of Reproductive Health, School of Public Health, Peking University, Beijing, China.
Source: Birth defects research. Part A, Clinical and molecular teratology [Birth Defects Res A Clin Mol Teratol] 2015 Jun; Vol. 103 (6), pp. 471-8. Date of Electronic Publication: 2014 Nov 05.
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Wiley Country of Publication: United States NLM ID: 101155107 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1542-0760 (Electronic) Linking ISSN: 15420752 NLM ISO Abbreviation: Birth Defects Res A Clin Mol Teratol Subsets: MEDLINE
Database: MEDLINE Ultimate
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ISSN:1542-0760
DOI:10.1002/bdra.23332