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Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics.
Kalia, Sarah S; Adelman, Kathy; Bale, Sherri J; Chung, Wendy K; Eng, Christine; Evans, James P; Herman, Gail E; Hufnagel, Sophia B; Klein, Teri E; Korf, Bruce R; McKelvey, Kent D; Ormond, Kelly E; Richards, C Sue; Vlangos, Christopher N; Watson, Michael; Martin, Christa L; Miller, David T.
Afiliação
  • Kalia SS; Division of Genetics, Brigham and Women's Hospital, Boston, Massachusetts, USA.
  • Adelman K; Patient advocate, Livermore, California, USA.
  • Bale SJ; GeneDx, Inc., Gaithersburg, Maryland, USA.
  • Chung WK; Department of Pediatrics, Columbia University, New York, New York, USA.
  • Eng C; Department of Medicine, Columbia University, New York, New York, USA.
  • Evans JP; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.
  • Herman GE; Department of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
  • Hufnagel SB; Institute for Genomic Medicine, Nationwide Children's Hospital and Department of Pediatrics, The Ohio State University, Columbus, Ohio, USA.
  • Klein TE; Division of Genetics and Metabolism, Children's National Health System, Washington, DC, USA.
  • Korf BR; Department of Genetics, Stanford University School of Medicine, Palo Alto, California, USA.
  • McKelvey KD; Department of Genetics, University of Alabama at Birmingham, Birmingham, Alabama, USA.
  • Ormond KE; Department of Genetics, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
  • Richards CS; Department of Family Medicine, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
  • Vlangos CN; Department of Genetics, Stanford University School of Medicine, Palo Alto, California, USA.
  • Watson M; Department of Molecular and Medical Genetics, Oregon Health & Science University, Portland, Oregon, USA.
  • Martin CL; Department of Pathology, Virginia Commonwealth University School of Medicine, Richmond, Virginia, USA.
  • Miller DT; American College of Medical Genetics and Genomics, Bethesda, Maryland, USA.
Genet Med ; 19(2): 249-255, 2017 02.
Article em En | MEDLINE | ID: mdl-27854360
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Genoma Humano / Testes Genéticos / Sequenciamento do Exoma / Genética Médica Tipo de estudo: Diagnostic_studies / Guideline / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2017 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: Genoma Humano / Testes Genéticos / Sequenciamento do Exoma / Genética Médica Tipo de estudo: Diagnostic_studies / Guideline / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article