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.

Affiliation

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 in En | MEDLINE | ID: mdl-31050105

Subject(s)

Genetic Testing/methods; Adult; Aged; Female; Genetic Predisposition to Disease; Humans; Male; Medical History Taking; Middle Aged; Uncertainty

Key words

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

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Genetic Testing Type of study: Prognostic_studies / Qualitative_research Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: J Genet Couns Journal subject: GENETICA MEDICA Year: 2019 Type: Article

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