Maternal vitamin use, infant C677T mutation in MTHFR, and isolated cleft palate risk

Am J Med Genet. 1999 Jul 2;85(1):84-5.
No abstract available

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • 5,10-Methylenetetrahydrofolate Reductase (FADH2)
  • Case-Control Studies
  • Cleft Palate / genetics*
  • Genotype
  • Humans
  • Infant, Newborn
  • Methylenetetrahydrofolate Reductase (NADPH2)
  • Mutation*
  • Oxidoreductases / genetics*
  • Risk Factors
  • Vitamins / administration & dosage*

Substances

  • Vitamins
  • Oxidoreductases
  • 5,10-Methylenetetrahydrofolate Reductase (FADH2)
  • Methylenetetrahydrofolate Reductase (NADPH2)