Infant methylenetetrahydrofolate reductase 677TT genotype is a risk factor for congenital heart disease

Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1. 1Congenital heart disease: A 10 year cohort1994 · 74 citations
2. 2Methylenetetrahydrofolate Reductase C677T Mutation, Plasma Homocysteine, and Folate in Subjects From Northern Italy With or Without Angiographically Documented Severe Coronary Atherosclerotic Disease: Evidence for an Important Genetic-Environmental Interaction1998 · 208 citations
3. 3Infant C677T mutation in MTHFR, maternal periconceptional vitamin use, and cleft lip1998 · 120 citations
4. 4A genetic defect in 5,10 methylenetetrahydrofolate reductase in neural tube defects1995 · 311 citations
5. 5Is the common 677C-->T mutation in the methylenetetrahydrofolate reductase gene a risk factor for neural tube defects? A meta-analysis1997 · 236 citations