Pular para o conteúdo
VuFind
    • English
    • Deutsch
    • Español
    • Français
    • Italiano
    • 日本語
    • Nederlands
    • Português
    • Português (Brasil)
    • 中文(简体)
    • 中文(繁體)
    • Türkçe
    • עברית
    • Gaeilge
    • Cymraeg
    • Ελληνικά
    • Català
    • Euskara
    • Русский
    • Čeština
    • Suomi
    • Svenska
    • polski
    • Dansk
    • slovenščina
    • اللغة العربية
    • বাংলা
    • Galego
    • Tiếng Việt
    • Hrvatski
    • हिंदी
    • Հայերէն
    • Українська
    • Sámegiella
    • Монгол
Avançada
  • Aetiological Role Of Folate De...
  • Citar
  • Enviar por SMS
  • Enviar por e-mail
  • Imprimir
  • Exportar registro
    • Exportar para RefWorks
    • Exportar para EndNoteWeb
    • Exportar para EndNote
  • Link permanente
Aetiological Role Of Folate Deficiency In Congenital Cardiovascular Malformation: Evidence From "Mendelian Randomisation" And Meta-Analysis

Aetiological Role Of Folate Deficiency In Congenital Cardiovascular Malformation: Evidence From "Mendelian Randomisation" And Meta-Analysis

Detalhes bibliográficos
Principais autores: Mamasoula, C, Pierscionek, T, Hall, D, Topf, A, Doza, J, Rahman, T, Tan, A, Bentham, J, Bhattacharya, S, Cosgrove, C, Brook, D, Riveron, J, Bu'Lock, F, O'Sullivan, J, Wren, C, Goodship, J, Cordell, H, Keavney, B
Formato: Conference item
Publicado em: 2012
  • Itens
  • Descrição
  • Registros relacionados
  • Registro fonte

Registros relacionados

  • Low-frequency intermediate penetrance variants in the ROCK1 gene predispose to Tetralogy of Fallot.
    por: Palomino Doza, J, et al.
    Publicado em: (2013)
  • A common variant in the PTPN11 gene contributes to the risk of tetralogy of Fallot.
    por: Goodship, J, et al.
    Publicado em: (2012)
  • Low-frequency intermediate penetrance variants in the ROCK1 gene predispose to congenital heart disease
    por: Palomino Doza, J, et al.
    Publicado em: (2012)
  • Genetic variation in VEGF does not contribute significantly to the risk of congenital cardiovascular malformation.
    por: Griffin, H, et al.
    Publicado em: (2009)
  • Association between C677T polymorphism of methylene tetrahydrofolate reductase and congenital heart disease: meta-analysis of 7697 cases and 13,125 controls.
    por: Mamasoula, C, et al.
    Publicado em: (2013)

Opções de Busca

  • Histórico de buscas
  • Busca Avançada

Encontrar Mais

  • Navegar o acervo
  • Navegar por ordem alfabética
  • Explorar canais
  • Bibliografia Recomendada
  • Novos itens

Precisa de ajuda?

  • Dicas de Busca
  • Serviço de Referência
  • Perguntas Frequentes