No evidence supporting MTHFR as a risk factor in the development of familial NSCLP
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference11 articles.
1. Role of the C677T polymorphism at theMTHFR gene on risk to nonsyndromic cleft lip with/without cleft palate: Results from a case-control study in Brazil
2. Methylenetetrahydrofolate reductase mutation and neural tube defects
3. Allele-Sharing Models: LOD Scores and Accurate Linkage Tests
4. Tests for Linkage and Association in Nuclear Families
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1. Folate pathway and nonsyndromic cleft lip and palate;Birth Defects Research Part A: Clinical and Molecular Teratology;2010-12-01
2. Nonsyndromic cleft lip and palate: CRISPLD genes and the folate gene pathway connection;Birth Defects Research Part A: Clinical and Molecular Teratology;2010-11-15
3. MTHFR,TGFB3, andTGFApolymorphisms and their association with the risk of non-syndromic cleft lip and cleft palate in China;American Journal of Medical Genetics Part A;2010-02
4. Development of the Craniofacial Complex;Bone and Development;2010
5. MTHFR 677TT Alone and IRF6 820GG Together with MTHFR 677CT, but Not MTHFR A1298C, Are Risks for Nonsyndromic Cleft Lip with or without Cleft Palate in an Indian Population;Genetic Testing and Molecular Biomarkers;2009-06
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