Impact of the MTHFR C677T polymorphism on risk of neural tube defects: case-control study

Παρόμοια τεκμήρια

• The Search for Genetic Polymorphisms in the Homocysteine/Folate Pathway That Contribute to the Etiology of Human Neural Tube Defects
  ανά: Molloy, Anne M., κ.ά.
  Έκδοση: (2009)
• Uncoupling Protein 2 Polymorphisms as Risk Factors for Neural Tube Defects
  ανά: Mitchell, Adam, κ.ά.
  Έκδοση: (2009)
• A Polymorphism, R653Q, in the Trifunctional Enzyme Methylenetetrahydrofolate Dehydrogenase/Methenyltetrahydrofolate Cyclohydrolase/Formyltetrahydrofolate Synthetase Is a Maternal Genetic Risk Factor for Neural Tube Defects: Report of the Birth Defects Research Group
  ανά: Brody, Lawrence C., κ.ά.
  Έκδοση: (2002)
• Maternal Vitamin B(12) Status and Risk of Neural Tube Defects in a Population With High Neural Tube Defect Prevalence and No Folic Acid Fortification
  ανά: Molloy, Anne M., κ.ά.
  Έκδοση: (2009)
• Transcobalamin II Receptor Polymorphisms Are Associated with Increased Risk for Neural Tube Defects
  ανά: Pangilinan, Faith, κ.ά.
  Έκδοση: (2010)