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Disclosure of cardiac variants of uncertain significance results in an exome cohort.
Lawal, T A; Lewis, K L; Johnston, J J; Heidlebaugh, A R; Ng, D; Gaston-Johansson, F G; Klein, W M P; Biesecker, B B; Biesecker, L G.
Afiliação
  • Lawal TA; National Institute of Nursing Research, National Institutes of Health (NIH), Bethesda, Maryland.
  • Lewis KL; Medical Genomics and Metabolic Genetics Branch, National Human Genome Research Institute, NIH, Bethesda, Maryland.
  • Johnston JJ; Medical Genomics and Metabolic Genetics Branch, National Human Genome Research Institute, NIH, Bethesda, Maryland.
  • Heidlebaugh AR; Social and Behavioral Research Branch, National Human Genome Research Institute, NIH, Bethesda, Maryland.
  • Ng D; Medical Genomics and Metabolic Genetics Branch, National Human Genome Research Institute, NIH, Bethesda, Maryland.
  • Gaston-Johansson FG; Department of Acute and Chronic Care, Johns Hopkins University School of Nursing, Baltimore, Maryland.
  • Klein WMP; Behavioral Research Program, National Cancer Institute, NIH, Bethesda, Maryland.
  • Biesecker BB; Social and Behavioral Research Branch, National Human Genome Research Institute, NIH, Bethesda, Maryland.
  • Biesecker LG; Medical Genomics and Metabolic Genetics Branch, National Human Genome Research Institute, NIH, Bethesda, Maryland.
Clin Genet ; 93(5): 1022-1029, 2018 05.
Article em En | MEDLINE | ID: mdl-29383714
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Contexto em Saúde: 2_ODS3 Problema de saúde: 2_muertes_prematuras_enfermedades_notrasmisibles Assunto principal: Predisposição Genética para Doença / Exoma / Cardiomiopatias Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male Idioma: En Revista: Clin Genet Ano de publicação: 2018 Tipo de documento: Article
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Contexto em Saúde: 2_ODS3 Problema de saúde: 2_muertes_prematuras_enfermedades_notrasmisibles Assunto principal: Predisposição Genética para Doença / Exoma / Cardiomiopatias Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male Idioma: En Revista: Clin Genet Ano de publicação: 2018 Tipo de documento: Article