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PhenomeCentral: 7 years of rare disease matchmaking.
Osmond, Matthew; Hartley, Taila; Johnstone, Brittney; Andjic, Sasha; Girdea, Marta; Gillespie, Meredith; Buske, Orion; Dumitriu, Sergiu; Koltunova, Veronika; Ramani, Arun; Boycott, Kym M; Brudno, Michael.
Afiliação
  • Osmond M; Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, ON, Canada.
  • Hartley T; Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, ON, Canada.
  • Johnstone B; Cancer Genetics and High Risk Program, Sunnybrook Health Sciences Centre and Department of Molecular Genetics, University of Toronto, Toronto, ON, Canada.
  • Andjic S; DATA Team and Techna Institute, University Health Network, Toronto, ON, Canada.
  • Girdea M; DATA Team and Techna Institute, University Health Network, Toronto, ON, Canada.
  • Gillespie M; Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, ON, Canada.
  • Buske O; PhenoTips, Toronto, ON, Canada.
  • Dumitriu S; DATA Team and Techna Institute, University Health Network, Toronto, ON, Canada.
  • Koltunova V; DATA Team and Techna Institute, University Health Network, Toronto, ON, Canada.
  • Ramani A; Centre for Computational Medicine, Hospital for Sick Children, Toronto, ON, Canada.
  • Boycott KM; Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, ON, Canada.
  • Brudno M; Department of Genetics, Children's Hospital of Eastern Ontario, Ottawa, ON, Canada.
Hum Mutat ; 43(6): 674-681, 2022 06.
Article em En | MEDLINE | ID: mdl-35165961
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Raras / Disseminação de Informação Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Revista: Hum Mutat Assunto da revista: GENETICA MEDICA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Canadá
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Raras / Disseminação de Informação Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Revista: Hum Mutat Assunto da revista: GENETICA MEDICA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Canadá