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Arachchi, Harindra; Wojcik, Monica H; Weisburd, Benjamin; Jacobsen, Julius O B; Valkanas, Elise; Baxter, Samantha; Byrne, Alicia B; O'Donnell-Luria, Anne H; Haendel, Melissa; Smedley, Damian; MacArthur, Daniel G; Philippakis, Anthony A; Rehm, Heidi L.
Afiliação
  • Arachchi H; Center for Mendelian Genomics, The Broad Institute of MIT and Harvard, Cambridge, Massachusetts.
  • Wojcik MH; The Broad Institute of MIT and Harvard, Cambridge, Massachusetts.
  • Weisburd B; Center for Mendelian Genomics, The Broad Institute of MIT and Harvard, Cambridge, Massachusetts.
  • Jacobsen JOB; Division of Genetics and Genomics, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts.
  • Valkanas E; Center for Mendelian Genomics, The Broad Institute of MIT and Harvard, Cambridge, Massachusetts.
  • Baxter S; William Harvey Research Institute, Barts & The London School of Medicine & Dentistry, Queen Mary University of London, Charterhouse Square, London, EC1M 6BQ, UK.
  • Byrne AB; Center for Mendelian Genomics, The Broad Institute of MIT and Harvard, Cambridge, Massachusetts.
  • O'Donnell-Luria AH; Center for Mendelian Genomics, The Broad Institute of MIT and Harvard, Cambridge, Massachusetts.
  • Haendel M; Center for Mendelian Genomics, The Broad Institute of MIT and Harvard, Cambridge, Massachusetts.
  • Smedley D; Department of Genetics and Molecular Pathology, Centre for Cancer Biology, SA Pathology, Adelaide, Australia.
  • MacArthur DG; School of Pharmacy and Medical Sciences, University of South Australia, Adelaide, Australia.
  • Philippakis AA; Center for Mendelian Genomics, The Broad Institute of MIT and Harvard, Cambridge, Massachusetts.
  • Rehm HL; Division of Genetics and Genomics, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts.
Hum Mutat ; 39(12): 1827-1834, 2018 12.
Article em En | MEDLINE | ID: mdl-30240502
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Armazenamento e Recuperação da Informação / Seleção de Pacientes / Doenças Raras Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Hum Mutat Assunto da revista: GENETICA MEDICA Ano de publicação: 2018 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Armazenamento e Recuperação da Informação / Seleção de Pacientes / Doenças Raras Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Hum Mutat Assunto da revista: GENETICA MEDICA Ano de publicação: 2018 Tipo de documento: Article