Understanding variants of uncertain significance in the era of multigene panels: Through the eyes of the patient.

Reuter, Chloe; Chun, Nicolette; Pariani, Mitchel; Hanson-Kahn, Andrea

Reuter, Chloe; Chun, Nicolette; Pariani, Mitchel; Hanson-Kahn, Andrea.

Afiliação

Reuter C; Stanford Center for Inherited Cardiovascular Disease, Division of Cardiovascular Medicine, Stanford School of Medicine, Stanford, California.
Chun N; Stanford Center for Undiagnosed Diseases, Division of Cardiovascular Medicine, Stanford School of Medicine, Stanford, California.
Pariani M; Cancer Genetics and Genomics, Stanford Health Care, Stanford, California.
Hanson-Kahn A; Stanford Center for Inherited Cardiovascular Disease, Division of Cardiovascular Medicine, Stanford School of Medicine, Stanford, California.

J Genet Couns ; 28(4): 878-886, 2019 08.

Article em En | MEDLINE | ID: mdl-31050105

Assuntos

Testes Genéticos/métodos; Adulto; Idoso; Feminino; Predisposição Genética para Doença; Humanos; Masculino; Anamnese; Pessoa de Meia-Idade; Incerteza

Palavras-chave

cancer genetics; genetic counseling; genetic testing; oncology; qualitative research; uncertainty; variant of uncertain significance

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Testes Genéticos Tipo de estudo: Prognostic_studies / Qualitative_research Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2019 Tipo de documento: Article

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