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Family Based Whole Exome Sequencing Reveals the Multifaceted Role of Notch Signaling in Congenital Heart Disease.
Preuss, Christoph; Capredon, Melanie; Wünnemann, Florian; Chetaille, Philippe; Prince, Andrea; Godard, Beatrice; Leclerc, Severine; Sobreira, Nara; Ling, Hua; Awadalla, Philip; Thibeault, Maryse; Khairy, Paul; Samuels, Mark E; Andelfinger, Gregor.
Afiliación
  • Preuss C; Cardiovascular Genetics, Department of Pediatrics, CHU Sainte-Justine, Université de Montréal, Montreal, Québec, Canada.
  • Capredon M; Cardiovascular Genetics, Department of Pediatrics, CHU Sainte-Justine, Université de Montréal, Montreal, Québec, Canada.
  • Wünnemann F; Cardiovascular Genetics, Department of Pediatrics, CHU Sainte-Justine, Université de Montréal, Montreal, Québec, Canada.
  • Chetaille P; Faculty of Biology, University of Muenster, Muenster, Germany.
  • Prince A; Department of Pediatrics, Centre Mère Enfants Soleil, Centre Hospitalier de l'Université (CHU) de Québec, Quebec City, Québec, Canada.
  • Godard B; Cardiovascular Genetics, Department of Pediatrics, CHU Sainte-Justine, Université de Montréal, Montreal, Québec, Canada.
  • Leclerc S; Omics-Ethics Research Group, Research Institute of Public Health, Université de Montréal, Montréal Québec, Canada.
  • Sobreira N; Cardiovascular Genetics, Department of Pediatrics, CHU Sainte-Justine, Université de Montréal, Montreal, Québec, Canada.
  • Ling H; McKusick Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.
  • Awadalla P; McKusick Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.
  • Thibeault M; Ontario Institute for Cancer Research, Toronto, Ontario, Canada.
  • Khairy P; Cardiovascular Genetics, Department of Pediatrics, CHU Sainte-Justine, Université de Montréal, Montreal, Québec, Canada.
  • Andelfinger G; Centre de Recherche CHU Sainte Justine, Université de Montreal, Montréal, Québec, Canada.
PLoS Genet ; 12(10): e1006335, 2016 Oct.
Article en En | MEDLINE | ID: mdl-27760138
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Obstrucción del Flujo Ventricular Externo / Constricción Patológica / Receptor Notch1 / Cardiopatías Congénitas Límite: Female / Humans / Male Idioma: En Revista: PLoS Genet Asunto de la revista: GENETICA Año: 2016 Tipo del documento: Article País de afiliación: Canadá
Texto completo
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Obstrucción del Flujo Ventricular Externo / Constricción Patológica / Receptor Notch1 / Cardiopatías Congénitas Límite: Female / Humans / Male Idioma: En Revista: PLoS Genet Asunto de la revista: GENETICA Año: 2016 Tipo del documento: Article País de afiliación: Canadá