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Exome sequencing identifies rare variants in multiple genes in atrioventricular septal defect.
D'Alessandro, Lisa C A; Al Turki, Saeed; Manickaraj, Ashok Kumar; Manase, Dorin; Mulder, Barbara J M; Bergin, Lynn; Rosenberg, Herschel C; Mondal, Tapas; Gordon, Elaine; Lougheed, Jane; Smythe, John; Devriendt, Koen; Bhattacharya, Shoumo; Watkins, Hugh; Bentham, Jamie; Bowdin, Sarah; Hurles, Matthew E; Mital, Seema.
Afiliación
  • D'Alessandro LC; Division of Cardiology, Department of Pediatrics, Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.
  • Al Turki S; Wellcome Trust Sanger Institute, Hinxton, Cambridge, UK.
  • Manickaraj AK; Department of Pathology, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
  • Manase D; Division of Cardiology, Department of Pediatrics, Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.
  • Mulder BJ; Division of Cardiology, Department of Pediatrics, Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.
  • Bergin L; Heart Center, Academic Medical Center, Amsterdam, The Netherlands.
  • Rosenberg HC; Division of Cardiology, Department of Medicine, London Health Sciences Centre, London, Ontario, Canada.
  • Mondal T; Department of Paediatrics, London Health Sciences Centre, London, Ontario, Canada.
  • Gordon E; Department of Pediatrics, Hamilton Health Sciences Centre, Hamilton, Ontario, Canada.
  • Lougheed J; Division of Cardiology, Department of Medicine, Hamilton Health Sciences Centre, Hamilton, Ontario, Canada.
  • Smythe J; Division of Cardiology, Department of Pediatrics, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.
  • Devriendt K; Department of Pediatrics, Kingston General Hospital, Kingston, Ontario, Canada.
  • Bhattacharya S; Centre for Human Genetics, Katholieke Universiteit Leuven, Leuven, Belgium.
  • Watkins H; Radcliffe Department of Medicine & Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK.
  • Bentham J; Radcliffe Department of Medicine & Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK.
  • Bowdin S; Department of Cardiology, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts USA.
  • Hurles ME; Division of Genetics, Department of Pediatrics, Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.
  • Mital S; Wellcome Trust Sanger Institute, Hinxton, Cambridge, UK.
Genet Med ; 18(2): 189-98, 2016 Feb.
Article en En | MEDLINE | ID: mdl-25996639
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Variación Genética / Exoma / Defectos de los Tabiques Cardíacos Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Female / Humans / Male Idioma: En Revista: Genet Med Asunto de la revista: GENETICA MEDICA Año: 2016 Tipo del documento: Article País de afiliación: Canadá
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Variación Genética / Exoma / Defectos de los Tabiques Cardíacos Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Female / Humans / Male Idioma: En Revista: Genet Med Asunto de la revista: GENETICA MEDICA Año: 2016 Tipo del documento: Article País de afiliación: Canadá