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Improving diagnostic precision, care and syndrome definitions using comprehensive next-generation sequencing for the inherited bone marrow failure syndromes.
Ghemlas, Ibrahim; Li, Hongbing; Zlateska, Bozana; Klaassen, Robert; Fernandez, Conrad V; Yanofsky, Rochelle A; Wu, John; Pastore, Yves; Silva, Mariana; Lipton, Jeff H; Brossard, Josee; Michon, Bruno; Abish, Sharon; Steele, MacGregor; Sinha, Roona; Belletrutti, Mark; Breakey, Vicky R; Jardine, Lawrence; Goodyear, Lisa; Sung, Lillian; Dhanraj, Santhosh; Reble, Emma; Wagner, Amanda; Beyene, Joseph; Ray, Peter; Meyn, Stephen; Cada, Michaela; Dror, Yigal.
Afiliação
  • Ghemlas I; Program in Genetics and Genome Biology, Research Institute, Toronto, Ontario, Canada Marrow Failure and Myelodysplasia Program, Division of Hematology/Oncology, Department of Paediatrics, The Hospital for Sick Children, Toronto, Ontario, Canada King Faisal Specialist Hospital and Research Center, Ri
  • Li H; Program in Genetics and Genome Biology, Research Institute, Toronto, Ontario, Canada.
  • Zlateska B; Program in Genetics and Genome Biology, Research Institute, Toronto, Ontario, Canada.
  • Klaassen R; Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.
  • Fernandez CV; IWK Health Centre, Halifax, Nova Scotia, Canada.
  • Yanofsky RA; CancerCare Manitoba, Winnipeg, Manitoba, Canada.
  • Wu J; British Columbia Children's Hospital, Vancouver, British Columbia, Canada.
  • Pastore Y; Hôpital Ste. Justine, Montréal, Québec, Canada.
  • Silva M; Queen's University, Kingston, Ontario, Canada.
  • Lipton JH; Princess Margaret Hospital, Toronto, Ontario, Canada.
  • Brossard J; Centre hospitalier universitaire, Sherbrooke, Quebec, Canada.
  • Michon B; Centre Hospital University Quebec-Pav CHUL, Sainte-Foy, Quebec, Canada.
  • Abish S; Montreal Children's Hospital, Montreal, Québec, Canada.
  • Steele M; Alberta Children's Hospital, Calgary, Alberta, Canada.
  • Sinha R; University of Saskatchewan, Saskatoon, Saskatchewan, Canada.
  • Belletrutti M; Stollery Children's Hospital, University of Alberta, Edmonton, Alberta, Canada.
  • Breakey VR; McMaster Children's Hospital, McMaster University, Hamilton, Ontario, Canada.
  • Jardine L; Children's Hospital at London Health Sciences Centre, London, Ontario, Canada.
  • Goodyear L; Janeway Child Health Centre, St. John's, Newfoundland, Canada.
  • Sung L; Population Health Sciences, Research Institute, The Hospital For Sick Children, Toronto, Ontario, Canada.
  • Dhanraj S; Program in Genetics and Genome Biology, Research Institute, Toronto, Ontario, Canada Faculty of Medicine, Institute of Medical Sciences, University of Toronto, Toronto, Ontario, Canada.
  • Reble E; Program in Genetics and Genome Biology, Research Institute, Toronto, Ontario, Canada.
  • Wagner A; Marrow Failure and Myelodysplasia Program, Division of Hematology/Oncology, Department of Paediatrics, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Beyene J; Program in Population Genomics, Department of Clinical Epidemiology & Biostatistics, Faculty of Health Sciences, McMaster University, Hamilton, Ontario, Canada.
  • Ray P; Program in Genetics and Genome Biology, Research Institute, Toronto, Ontario, Canada Molecular Genetic Laboratory, Department of Paediatric Laboratory Medicine, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Meyn S; Program in Genetics and Genome Biology, Research Institute, Toronto, Ontario, Canada.
  • Cada M; Marrow Failure and Myelodysplasia Program, Division of Hematology/Oncology, Department of Paediatrics, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Dror Y; Program in Genetics and Genome Biology, Research Institute, Toronto, Ontario, Canada Marrow Failure and Myelodysplasia Program, Division of Hematology/Oncology, Department of Paediatrics, The Hospital for Sick Children, Toronto, Ontario, Canada Faculty of Medicine, Institute of Medical Sciences, Uni
J Med Genet ; 52(9): 575-84, 2015 Sep.
Article em En | MEDLINE | ID: mdl-26136524
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Análise de Sequência de DNA / Hemoglobinúria Paroxística Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2015 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Análise de Sequência de DNA / Hemoglobinúria Paroxística Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2015 Tipo de documento: Article