Evaluation of C677T and A1298C polymorphisms of theMTHFRgene as maternal risk factors for Down syndrome and congenital heart defects
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.32989/fullpdf
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3. The meiotic stage of nondisjunction in trisomy 21: Determination by using DNA polymorphisms;Antonarakis;Am J Hum Genet,1992
4. Prevalence of the mutation C677 → T in the methylene tetrahydrofolate reductase gene among distinct ethnic groups in Brazil;Arruda;Am J Med Genet,1998
5. DNA methylation in folate deficiency: Use of CpG methylase;Balaghi;Biochem Biophys Res Commun,1993
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