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High-frequency actionable pathogenic exome variants in an average-risk cohort.
Rego, Shannon; Dagan-Rosenfeld, Orit; Zhou, Wenyu; Sailani, M Reza; Limcaoco, Patricia; Colbert, Elizabeth; Avina, Monika; Wheeler, Jessica; Craig, Colleen; Salins, Denis; Röst, Hannes L; Dunn, Jessilyn; McLaughlin, Tracey; Steinmetz, Lars M; Bernstein, Jonathan A; Snyder, Michael P.
Afiliação
  • Rego S; Department of Genetics, Stanford University School of Medicine, Stanford, California 94305, USA.
  • Dagan-Rosenfeld O; Department of Genetics, Stanford University School of Medicine, Stanford, California 94305, USA.
  • Zhou W; Department of Genetics, Stanford University School of Medicine, Stanford, California 94305, USA.
  • Sailani MR; Department of Genetics, Stanford University School of Medicine, Stanford, California 94305, USA.
  • Limcaoco P; Department of Genetics, Stanford University School of Medicine, Stanford, California 94305, USA.
  • Colbert E; Department of Medicine, Stanford University School of Medicine, Stanford, California 94305, USA.
  • Avina M; Department of Genetics, Stanford University School of Medicine, Stanford, California 94305, USA.
  • Wheeler J; Department of Genetics, Stanford University School of Medicine, Stanford, California 94305, USA.
  • Craig C; Department of Medicine, Stanford University School of Medicine, Stanford, California 94305, USA.
  • Salins D; Department of Genetics, Stanford University School of Medicine, Stanford, California 94305, USA.
  • Röst HL; Department of Genetics, Stanford University School of Medicine, Stanford, California 94305, USA.
  • Dunn J; Department of Genetics, Stanford University School of Medicine, Stanford, California 94305, USA.
  • McLaughlin T; Mobilize Center, Stanford University, Stanford, California 94305, USA.
  • Steinmetz LM; Department of Medicine, Stanford University School of Medicine, Stanford, California 94305, USA.
  • Bernstein JA; Department of Genetics, Stanford University School of Medicine, Stanford, California 94305, USA.
  • Snyder MP; Stanford Genome Technology Center, Stanford University, Palo Alto, California 94304, USA.
Article em En | MEDLINE | ID: mdl-30487145

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Achados Incidentais / Sequenciamento do Exoma Tipo de estudo: Diagnostic_studies / Etiology_studies / Guideline / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Achados Incidentais / Sequenciamento do Exoma Tipo de estudo: Diagnostic_studies / Etiology_studies / Guideline / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male Idioma: En Ano de publicação: 2018 Tipo de documento: Article