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2. Evaluation of infant methylenetetrahydrofolate reductase genotype, maternal vitamin use, and risk of high versus low level spina bifida defects. Volcik KA; Shaw GM; Lammer EJ; Zhu H; Finnell RH Birth Defects Res A Clin Mol Teratol; 2003 Mar; 67(3):154-7. PubMed ID: 12797455 [TBL] [Abstract][Full Text] [Related]
3. [Study of correlationship between congenital heart disease and 5, 10-methylenetetra hydrofolate reductase gene's polymorphism or folacin intakes]. Li D; Jing XA; Wang HY; Ye WJ; Fan H Zhonghua Yu Fang Yi Xue Za Zhi; 2009 Aug; 43(8):700-4. PubMed ID: 20021850 [TBL] [Abstract][Full Text] [Related]
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12. Association of congenital cardiac defects and the C677T methylenetetrahydrofolate reductase polymorphism. Wintner S; Hafner E; Stonek F; Stuempflen I; Metzenbauer M; Philipp K Prenat Diagn; 2007 Aug; 27(8):704-8. PubMed ID: 17510921 [TBL] [Abstract][Full Text] [Related]
13. Common C677T polymorphism of the methylenetetrahydrofolate reductase gene and the risk of venous thromboembolism: meta-analysis of 31 studies. Ray JG; Shmorgun D; Chan WS Pathophysiol Haemost Thromb; 2002; 32(2):51-8. PubMed ID: 12214149 [TBL] [Abstract][Full Text] [Related]
14. Association of the C677T methylenetetrahydrofolate reductase mutation with congenital heart diseases. Lee CN; Su YN; Cheng WF; Lin MT; Wang JK; Wu MH; Hsieh FJ Acta Obstet Gynecol Scand; 2005 Dec; 84(12):1134-40. PubMed ID: 16305696 [TBL] [Abstract][Full Text] [Related]
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