MTHFR rs2274976 polymorphism is a risk marker for nonsyndromic cleft lip with or without cleft palate in the brazilian population

MTHFR rs2274976 polymorphism is a risk marker for nonsyndromic cleft lip with or without cleft palate in the brazilian population

S. N. De Aquino, R. Hoshi, E. Bagordakis, M.G.R. Pucciarelli, A.C. Messetti, H. Moreira, A. Bufalino, A. Borges, A.L. Rangel, L.A. Brito, M.S.O Swerts, H. Martelli-Junior, S.R. Line, E. Graner, S.R.A. Reis, M.R. Passos-Bueno, R.D. Coletta

ARTIGO

Inglês

BackgroundPolymorphisms within the MTHFR (rs2274976) and MTHFD1 (rs2236225) genes were previously associated with maternal susceptibility for having an offspring with nonsyndromic cleft lip with or without cleft palate (NSCL/P) in the Brazilian population. However, as the genotypes of the patients...

Polymorphisms within the MTHFR (rs2274976) and MTHFD1 (rs2236225) genes were previously associated with maternal susceptibility for having an offspring with nonsyndromic cleft lip with or without cleft palate (NSCL/P) in the Brazilian population. However,

CONSELHO NACIONAL DE DESENVOLVIMENTO CIENTÍFICO E TECNOLÓGICO - CNPQ

FUNDAÇÃO DE AMPARO À PESQUISA DO ESTADO DE SÃO PAULO - FAPESP

COORDENAÇÃO DE APERFEIÇOAMENTO DE PESSOAL DE NÍVEL SUPERIOR - CAPES

FUNDAÇÃO DE AMPARO À PESQUISA DO ESTADO DE MINA

Fechado

MTHFR rs2274976 polymorphism is a risk marker for nonsyndromic cleft lip with or without cleft palate in the brazilian population

S. N. De Aquino, R. Hoshi, E. Bagordakis, M.G.R. Pucciarelli, A.C. Messetti, H. Moreira, A. Bufalino, A. Borges, A.L. Rangel, L.A. Brito, M.S.O Swerts, H. Martelli-Junior, S.R. Line, E. Graner, S.R.A. Reis, M.R. Passos-Bueno, R.D. Coletta


										

MTHFR rs2274976 polymorphism is a risk marker for nonsyndromic cleft lip with or without cleft palate in the brazilian population

S. N. De Aquino, R. Hoshi, E. Bagordakis, M.G.R. Pucciarelli, A.C. Messetti, H. Moreira, A. Bufalino, A. Borges, A.L. Rangel, L.A. Brito, M.S.O Swerts, H. Martelli-Junior, S.R. Line, E. Graner, S.R.A. Reis, M.R. Passos-Bueno, R.D. Coletta

    Fontes

    Birth defects research. Part A: clinical and molecular teratology

    Vol. 100, no. 1 (jan., 2014), p. 30-35