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Two MTHFR polymorphisms, maternal B-vitamin intake, and CHDs.
van Driel LM, Verkleij-Hagoort AC, de Jonge R, Uitterlinden AG, Steegers EA, van Duijn CM, Steegers-Theunissen RP. van Driel LM, et al. Among authors: verkleij hagoort ac. Birth Defects Res A Clin Mol Teratol. 2008 Jun;82(6):474-81. doi: 10.1002/bdra.20463. Birth Defects Res A Clin Mol Teratol. 2008. PMID: 18452180
Maternal hyperhomocysteinaemia is a risk factor for congenital heart disease.
Verkleij-Hagoort AC, Verlinde M, Ursem NT, Lindemans J, Helbing WA, Ottenkamp J, Siebel FM, Gittenberger-de Groot AC, de Jonge R, Bartelings MM, Steegers EA, Steegers-Theunissen RP. Verkleij-Hagoort AC, et al. BJOG. 2006 Dec;113(12):1412-8. doi: 10.1111/j.1471-0528.2006.01109.x. BJOG. 2006. PMID: 17081182
Phenotypic variability of atypical 22q11.2 deletions not including TBX1.
Verhagen JM, Diderich KE, Oudesluijs G, Mancini GM, Eggink AJ, Verkleij-Hagoort AC, Groenenberg IA, Willems PJ, du Plessis FA, de Man SA, Srebniak MI, van Opstal D, Hulsman LO, van Zutven LJ, Wessels MW. Verhagen JM, et al. Among authors: verkleij hagoort ac. Am J Med Genet A. 2012 Oct;158A(10):2412-20. doi: 10.1002/ajmg.a.35517. Epub 2012 Aug 14. Am J Med Genet A. 2012. PMID: 22893440
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