Your browser doesn't support javascript.
loading
Determining the association between methylenetetrahydrofolate reductase (MTHFR) gene polymorphisms and genomic DNA methylation level: A meta-analysis.
Wang, Li; Shangguan, Shaofang; Chang, Shaoyan; Yu, Xin; Wang, Zhen; Lu, Xiaolin; Wu, Lihua; Zhang, Ting.
Affiliation
  • Wang L; Beijing Municipal Key Laboratory of Child Development and Nutriomics, Capital Institute of Pediatrics, Beijing, China.
  • Shangguan S; Beijing Municipal Key Laboratory of Child Development and Nutriomics, Capital Institute of Pediatrics, Beijing, China.
  • Chang S; Beijing Municipal Key Laboratory of Child Development and Nutriomics, Capital Institute of Pediatrics, Beijing, China.
  • Yu X; Beijing Municipal Key Laboratory of Child Development and Nutriomics, Capital Institute of Pediatrics, Beijing, China.
  • Wang Z; Beijing Municipal Key Laboratory of Child Development and Nutriomics, Capital Institute of Pediatrics, Beijing, China.
  • Lu X; Beijing Municipal Key Laboratory of Child Development and Nutriomics, Capital Institute of Pediatrics, Beijing, China.
  • Wu L; Beijing Municipal Key Laboratory of Child Development and Nutriomics, Capital Institute of Pediatrics, Beijing, China.
  • Zhang T; Beijing Municipal Key Laboratory of Child Development and Nutriomics, Capital Institute of Pediatrics, Beijing, China.
Birth Defects Res A Clin Mol Teratol ; 106(8): 667-74, 2016 Aug.
Article in En | MEDLINE | ID: mdl-27173682

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DNA Methylation / Polymorphism, Single Nucleotide / Methylenetetrahydrofolate Reductase (NADPH2) / Neural Tube Defects Type of study: Diagnostic_studies / Etiology_studies / Risk_factors_studies / Systematic_reviews Limits: Female / Humans / Male Language: En Journal: Birth Defects Res A Clin Mol Teratol Year: 2016 Document type: Article Affiliation country: China Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DNA Methylation / Polymorphism, Single Nucleotide / Methylenetetrahydrofolate Reductase (NADPH2) / Neural Tube Defects Type of study: Diagnostic_studies / Etiology_studies / Risk_factors_studies / Systematic_reviews Limits: Female / Humans / Male Language: En Journal: Birth Defects Res A Clin Mol Teratol Year: 2016 Document type: Article Affiliation country: China Country of publication: United States