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Gene-based analyses of the maternal genome implicate maternal effect genes as risk factors for conotruncal heart defects.
Sewda, Anshuman; Agopian, A J; Goldmuntz, Elizabeth; Hakonarson, Hakon; Morrow, Bernice E; Musfee, Fadi; Taylor, Deanne; Mitchell, Laura E.
Afiliación
  • Sewda A; Department of Epidemiology, Human Genetics and Environmental Sciences, UTHealth School of Public Health, Houston, Texas, United States of America.
  • Agopian AJ; Department of Epidemiology, Human Genetics and Environmental Sciences, UTHealth School of Public Health, Houston, Texas, United States of America.
  • Goldmuntz E; Department of Pediatrics, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, United States of America.
  • Hakonarson H; Division of Cardiology, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, United States of America.
  • Morrow BE; Department of Pediatrics, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, United States of America.
  • Musfee F; Center for Applied Genomics, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, United States of America.
  • Taylor D; Department of Genetics, Albert Einstein College of Medicine, Bronx, New York, United States of America.
  • Mitchell LE; Department of Epidemiology, Human Genetics and Environmental Sciences, UTHealth School of Public Health, Houston, Texas, United States of America.
PLoS One ; 15(6): e0234357, 2020.
Article en En | MEDLINE | ID: mdl-32516339
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 2_ODS3 Problema de salud: 2_muertes_prematuras_enfermedades_notrasmisibles Asunto principal: Herencia Materna / Cardiopatías Congénitas Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Child, preschool / Female / Humans / Infant / Male / Middle aged / Newborn / Pregnancy Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 2_ODS3 Problema de salud: 2_muertes_prematuras_enfermedades_notrasmisibles Asunto principal: Herencia Materna / Cardiopatías Congénitas Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Child, preschool / Female / Humans / Infant / Male / Middle aged / Newborn / Pregnancy Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos