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ModelMatcher: A scientist-centric online platform to facilitate collaborations between stakeholders of rare and undiagnosed disease research.
Harnish, J Michael; Li, Lucian; Rogic, Sanja; Poirier-Morency, Guillaume; Kim, Seon-Young; Boycott, Kym M; Wangler, Michael F; Bellen, Hugo J; Hieter, Philip; Pavlidis, Paul; Liu, Zhandong; Yamamoto, Shinya.
Afiliação
  • Harnish JM; Department of Molecular and Human Genetics, Baylor College of Medicine (BCM), Houston, Texas, USA.
  • Li L; Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital (TCH), Houston, Texas, USA.
  • Rogic S; Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital (TCH), Houston, Texas, USA.
  • Poirier-Morency G; Department of Pediatrics, Division of Neurology and Developmental Neuroscience, BCM, Houston, Texas, USA.
  • Kim SY; Michael Smith Laboratories, University of British Columbia, Vancouver, British Columbia, Canada.
  • Boycott KM; Michael Smith Laboratories, University of British Columbia, Vancouver, British Columbia, Canada.
  • Wangler MF; Department of Psychiatry, University of British Columbia, Vancouver, British Columbia, Canada.
  • Bellen HJ; Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital (TCH), Houston, Texas, USA.
  • Hieter P; Department of Pediatrics, Division of Neurology and Developmental Neuroscience, BCM, Houston, Texas, USA.
  • Liu Z; Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Ontario, Canada.
  • Yamamoto S; Department of Molecular and Human Genetics, Baylor College of Medicine (BCM), Houston, Texas, USA.
Hum Mutat ; 43(6): 743-759, 2022 06.
Article em En | MEDLINE | ID: mdl-35224820
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças não Diagnosticadas 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: Estados Unidos
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças não Diagnosticadas 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: Estados Unidos