Studies of reduced folate carrier 1 (RFC1) A80G and 5,10-methylenetetrahydrofolate reductase (MTHFR) C677T polymorphisms with neural tube and orofacial cleft defects

Am J Med Genet A. 2005 Jun 1;135(2):220-3. doi: 10.1002/ajmg.a.30705.
No abstract available

Publication types

  • Comparative Study
  • Letter
  • Multicenter Study
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Alleles
  • Cleft Lip / genetics*
  • Cleft Palate / genetics*
  • Family Health
  • Female
  • Gene Frequency
  • Genotype
  • Humans
  • Linkage Disequilibrium
  • Male
  • Membrane Transport Proteins / genetics*
  • Methylenetetrahydrofolate Reductase (NADPH2) / genetics*
  • Neural Tube Defects / genetics*
  • Pedigree
  • Point Mutation
  • Polymorphism, Genetic*

Substances

  • Membrane Transport Proteins
  • SLC19A2 protein, human
  • Methylenetetrahydrofolate Reductase (NADPH2)