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A toolkit for genetics providers in follow-up of patients with non-diagnostic exome sequencing.
Zastrow, Diane B; Kohler, Jennefer N; Bonner, Devon; Reuter, Chloe M; Fernandez, Liliana; Grove, Megan E; Fisk, Dianna G; Yang, Yaping; Eng, Christine M; Ward, Patricia A; Bick, David; Worthey, Elizabeth A; Fisher, Paul G; Ashley, Euan A; Bernstein, Jonathan A; Wheeler, Matthew T.
Afiliação
  • Zastrow DB; Center for Undiagnosed Diseases, Stanford University, Stanford, California.
  • Kohler JN; Center for Undiagnosed Diseases, Stanford University, Stanford, California.
  • Bonner D; Center for Undiagnosed Diseases, Stanford University, Stanford, California.
  • Reuter CM; Center for Undiagnosed Diseases, Stanford University, Stanford, California.
  • Fernandez L; Center for Undiagnosed Diseases, Stanford University, Stanford, California.
  • Grove ME; Clinical Genomics Program, Stanford Health Care, Stanford, California.
  • Fisk DG; Clinical Genomics Program, Stanford Health Care, Stanford, California.
  • Yang Y; Baylor College of Medicine, Houston, Texas.
  • Eng CM; Baylor College of Medicine, Houston, Texas.
  • Ward PA; Baylor College of Medicine, Houston, Texas.
  • Bick D; HudsonAlpha Institute for Biotechnology, Huntsville, Alabama.
  • Worthey EA; HudsonAlpha Institute for Biotechnology, Huntsville, Alabama.
  • Fisher PG; Center for Undiagnosed Diseases, Stanford University, Stanford, California.
  • Ashley EA; Department of Neurology, Stanford University School of Medicine, Stanford, California.
  • Bernstein JA; Department of Pediatrics, Stanford University School of Medicine, Stanford, California.
  • Wheeler MT; Center for Undiagnosed Diseases, Stanford University, Stanford, California.
J Genet Couns ; 28(2): 213-228, 2019 04.
Article em En | MEDLINE | ID: mdl-30964584
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Raras / Sequenciamento do Exoma / Doenças não Diagnosticadas Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies Limite: Female / Humans / Male Idioma: En Revista: J Genet Couns Assunto da revista: GENETICA MEDICA Ano de publicação: 2019 Tipo de documento: Article País de publicação: Estados Unidos
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Raras / Sequenciamento do Exoma / Doenças não Diagnosticadas Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies Limite: Female / Humans / Male Idioma: En Revista: J Genet Couns Assunto da revista: GENETICA MEDICA Ano de publicação: 2019 Tipo de documento: Article País de publicação: Estados Unidos