Absence of association of fetal MTHFR C677T polymorphism with prenatal Down syndrome pregnancies

Eur J Hum Genet. 2003 Jan;11(1):5. doi: 10.1038/sj.ejhg.5200928.
No abstract available

Publication types

  • Letter
  • Comment

MeSH terms

  • Down Syndrome / genetics*
  • Female
  • Fetal Diseases / genetics
  • Homozygote
  • Humans
  • Methylenetetrahydrofolate Reductase (NADPH2)
  • Oxidoreductases Acting on CH-NH Group Donors / genetics*
  • Polymorphism, Genetic*
  • Pregnancy
  • White People / genetics

Substances

  • Oxidoreductases Acting on CH-NH Group Donors
  • Methylenetetrahydrofolate Reductase (NADPH2)