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The clinical application of genome-wide sequencing for monogenic diseases in Canada: Position Statement of the Canadian College of Medical Geneticists.
Boycott, Kym; Hartley, Taila; Adam, Shelin; Bernier, Francois; Chong, Karen; Fernandez, Bridget A; Friedman, Jan M; Geraghty, Michael T; Hume, Stacey; Knoppers, Bartha M; Laberge, Anne-Marie; Majewski, Jacek; Mendoza-Londono, Roberto; Meyn, M Stephen; Michaud, Jacques L; Nelson, Tanya N; Richer, Julie; Sadikovic, Bekim; Skidmore, David L; Stockley, Tracy; Taylor, Sherry; van Karnebeek, Clara; Zawati, Ma'n H; Lauzon, Julie; Armour, Christine M.
Afiliación
  • Boycott K; Children's Hospital of Eastern Ontario Research Institute, Ottawa, Ontario, Canada.
  • Hartley T; Children's Hospital of Eastern Ontario Research Institute, Ottawa, Ontario, Canada.
  • Adam S; Department of Medical Genetics, University of British Columbia, Vancouver, British Columbia, Canada.
  • Bernier F; Department of Medical Genetics, University of Calgary, Calgary, Alberta, Canada.
  • Chong K; The Hospital for Sick Children and University of Toronto, Toronto, Ontario, Canada Prenatal Diagnosis and Medical Genetics Program, Mount Sinai Hospital, Toronto, Ontario, Canada.
  • Fernandez BA; Disciplines of Genetics and Medicine, Faculty of Medicine, Memorial University of Newfoundland, St. John's, Newfoundland, Canada.
  • Friedman JM; Department of Medical Genetics, University of British Columbia, Vancouver, British Columbia, Canada.
  • Geraghty MT; Children's Hospital of Eastern Ontario Research Institute, Ottawa, Ontario, Canada.
  • Hume S; University of Alberta, Edmonton, Alberta, Canada.
  • Knoppers BM; McGill University and Centre of Genomics and Policy, Montréal, Québec, Canada.
  • Laberge AM; Centre de Recherche du Centre Hospitalier Universitaire Sainte-Justine and Departments of Pediatrics and Neurosciences, Université de Montréal, Montréal, Québec, Canada.
  • Majewski J; Department of Human Genetics, McGill University, Montréal, Québec, Canada.
  • Mendoza-Londono R; The Hospital for Sick Children and University of Toronto, Toronto, Ontario, Canada.
  • Meyn MS; The Hospital for Sick Children and University of Toronto, Toronto, Ontario, Canada The Program in Genetics and Genome Biology, Hospital for Sick Children, Toronto, Ontario, Canada.
  • Michaud JL; Centre de Recherche du Centre Hospitalier Universitaire Sainte-Justine and Departments of Pediatrics and Neurosciences, Université de Montréal, Montréal, Québec, Canada.
  • Nelson TN; Department of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
  • Richer J; Children's Hospital of Eastern Ontario Research Institute, Ottawa, Ontario, Canada.
  • Sadikovic B; Department of Pathology and Laboratory Medicine, Western University, London, Ontario, Canada.
  • Skidmore DL; Maritime Medical Genetics Program, Department of Pediatrics, Dalhousie University, Halifax, Nova Scotia, Canada.
  • Stockley T; Division of Molecular Genetics, Department of Pathology, University Health Network, Toronto, Ontario, Canada.
  • Taylor S; University of Alberta, Edmonton, Alberta, Canada.
  • van Karnebeek C; Department of Medical Genetics, University of British Columbia, Vancouver, British Columbia, Canada.
  • Zawati MH; McGill University and Centre of Genomics and Policy, Montréal, Québec, Canada.
  • Lauzon J; Department of Medical Genetics, University of Calgary, Calgary, Alberta, Canada.
  • Armour CM; Children's Hospital of Eastern Ontario Research Institute, Ottawa, Ontario, Canada.
J Med Genet ; 52(7): 431-7, 2015 Jul.
Article en En | MEDLINE | ID: mdl-25951830
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Genoma Humano / Análisis de Secuencia de ADN / Investigación Biomédica Traslacional / Genética Médica / Enfermedades Genéticas Congénitas Tipo de estudio: Guideline / Qualitative_research Límite: Humans País/Región como asunto: America do norte Idioma: En Revista: J Med Genet Año: 2015 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: Genoma Humano / Análisis de Secuencia de ADN / Investigación Biomédica Traslacional / Genética Médica / Enfermedades Genéticas Congénitas Tipo de estudio: Guideline / Qualitative_research Límite: Humans País/Región como asunto: America do norte Idioma: En Revista: J Med Genet Año: 2015 Tipo del documento: Article País de afiliación: Canadá