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Genome-wide association study of maternal and inherited effects on left-sided cardiac malformations.
Mitchell, Laura E; Agopian, A J; Bhalla, Angela; Glessner, Joseph T; Kim, Cecilia E; Swartz, Michael D; Hakonarson, Hakon; Goldmuntz, Elizabeth.
Afiliação
  • Mitchell LE; Division of Epidemiology, Human Genetics and Environmental Sciences, University of Texas School of Public Health, Houston, TX 77030, USA laura.e.mitchell@uth.tmc.edu.
  • Agopian AJ; Division of Epidemiology, Human Genetics and Environmental Sciences, University of Texas School of Public Health, Houston, TX 77030, USA.
  • Bhalla A; Division of Epidemiology, Human Genetics and Environmental Sciences, University of Texas School of Public Health, Houston, TX 77030, USA.
  • Glessner JT; The Center for Applied Genomics and.
  • Kim CE; The Center for Applied Genomics and.
  • Swartz MD; Division of Biostatistics, University of Texas School of Public Health, Houston, TX 77030, USA and.
  • Hakonarson H; The Center for Applied Genomics and Department of Pediatrics, The Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
  • Goldmuntz E; Division of Cardiology, The Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA Department of Pediatrics, The Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Hum Mol Genet ; 24(1): 265-73, 2015 Jan 01.
Article em En | MEDLINE | ID: mdl-25138779
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 10 / Cromossomos Humanos Par 16 / Sinaptofisina / Estudo de Associação Genômica Ampla / Cardiopatias Congênitas Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male / Pregnancy Idioma: En Ano de publicação: 2015 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 10 / Cromossomos Humanos Par 16 / Sinaptofisina / Estudo de Associação Genômica Ampla / Cardiopatias Congênitas Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male / Pregnancy Idioma: En Ano de publicação: 2015 Tipo de documento: Article