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RAPIDOMICS: rapid genome-wide sequencing in a neonatal intensive care unit-successes and challenges.
Elliott, Alison M; du Souich, Christèle; Lehman, Anna; Guella, Ilaria; Evans, Daniel M; Candido, Tara; Tooman, Leah; Armstrong, Linlea; Clarke, Lorne; Gibson, William; Gill, Harinder; Lavoie, Pascal M; Lewis, Suzanne; McKinnon, Margaret L; Nikkel, Sarah M; Patel, Millan; Solimano, Alfonso; Synnes, Anne; Ting, Joseph; van Allen, Margot; Christilaw, Jan; Farrer, Matthew J; Friedman, Jan M; Osiovich, Horacio.
Afiliación
  • Elliott AM; Department of Medical Genetics, University of British Columbia, Vancouver, Canada. alison.elliott@cw.bc.ca.
  • du Souich C; Provincial Medical Genetics Program, BC Women's Hospital and Health Centre, 4500 Oak Street, Vancouver, British Columbia, V6H 3N1, Canada. alison.elliott@cw.bc.ca.
  • Lehman A; Department of Medical Genetics, University of British Columbia, Vancouver, Canada.
  • Guella I; Provincial Medical Genetics Program, BC Women's Hospital and Health Centre, 4500 Oak Street, Vancouver, British Columbia, V6H 3N1, Canada.
  • Evans DM; Department of Medical Genetics, University of British Columbia, Vancouver, Canada.
  • Candido T; Provincial Medical Genetics Program, BC Women's Hospital and Health Centre, 4500 Oak Street, Vancouver, British Columbia, V6H 3N1, Canada.
  • Tooman L; Centre for Applied Neurogenetics, University of British Columbia, Vancouver, Canada.
  • Armstrong L; Centre for Applied Neurogenetics, University of British Columbia, Vancouver, Canada.
  • Clarke L; Centre for Applied Neurogenetics, University of British Columbia, Vancouver, Canada.
  • Gibson W; Centre for Applied Neurogenetics, University of British Columbia, Vancouver, Canada.
  • Gill H; Department of Medical Genetics, University of British Columbia, Vancouver, Canada.
  • Lavoie PM; Provincial Medical Genetics Program, BC Women's Hospital and Health Centre, 4500 Oak Street, Vancouver, British Columbia, V6H 3N1, Canada.
  • Lewis S; Department of Medical Genetics, University of British Columbia, Vancouver, Canada.
  • McKinnon ML; Provincial Medical Genetics Program, BC Women's Hospital and Health Centre, 4500 Oak Street, Vancouver, British Columbia, V6H 3N1, Canada.
  • Nikkel SM; Department of Medical Genetics, University of British Columbia, Vancouver, Canada.
  • Patel M; Provincial Medical Genetics Program, BC Women's Hospital and Health Centre, 4500 Oak Street, Vancouver, British Columbia, V6H 3N1, Canada.
  • Solimano A; Department of Medical Genetics, University of British Columbia, Vancouver, Canada.
  • Synnes A; Provincial Medical Genetics Program, BC Women's Hospital and Health Centre, 4500 Oak Street, Vancouver, British Columbia, V6H 3N1, Canada.
  • Ting J; Division of Neonatology, Department of Paediatrics, University of British Columbia, Vancouver, Canada.
  • van Allen M; Department of Medical Genetics, University of British Columbia, Vancouver, Canada.
  • Christilaw J; Provincial Medical Genetics Program, BC Women's Hospital and Health Centre, 4500 Oak Street, Vancouver, British Columbia, V6H 3N1, Canada.
  • Farrer MJ; Department of Medical Genetics, University of British Columbia, Vancouver, Canada.
  • Friedman JM; Provincial Medical Genetics Program, BC Women's Hospital and Health Centre, 4500 Oak Street, Vancouver, British Columbia, V6H 3N1, Canada.
  • Osiovich H; Department of Medical Genetics, University of British Columbia, Vancouver, Canada.
Eur J Pediatr ; 178(8): 1207-1218, 2019 Aug.
Article en En | MEDLINE | ID: mdl-31172278
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Unidades de Cuidado Intensivo Neonatal / Cuidado Intensivo Neonatal / Pruebas Genéticas / Secuenciación del Exoma / Enfermedades Genéticas Congénitas Tipo de estudio: Prognostic_studies Límite: Female / Humans / Male / Newborn Idioma: En Año: 2019 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Unidades de Cuidado Intensivo Neonatal / Cuidado Intensivo Neonatal / Pruebas Genéticas / Secuenciación del Exoma / Enfermedades Genéticas Congénitas Tipo de estudio: Prognostic_studies Límite: Female / Humans / Male / Newborn Idioma: En Año: 2019 Tipo del documento: Article