Identifying sequence variants contributing to hereditary breast and ovarian cancer in BRCA1 and BRCA2 negative breast and ovarian cancer patients.

Jarhelle, Elisabeth; Riise Stensland, Hilde Monica Frostad; Hansen, Geir Åsmund Myge; Skarsfjord, Siri; Jonsrud, Christoffer; Ingebrigtsen, Monica; Strømsvik, Nina; Van Ghelue, Marijke

Identifying sequence variants contributing to hereditary breast and ovarian cancer in BRCA1 and BRCA2 negative breast and ovarian cancer patients.

Jarhelle, Elisabeth; Riise Stensland, Hilde Monica Frostad; Hansen, Geir Åsmund Myge; Skarsfjord, Siri; Jonsrud, Christoffer; Ingebrigtsen, Monica; Strømsvik, Nina; Van Ghelue, Marijke.

Afiliación

Jarhelle E; Department of Medical Genetics, Division of Child and Adolescent Health, University Hospital of North Norway, Tromsø, Norway. elisabeth.jarhelle@unn.no.
Riise Stensland HMF; Department of Clinical Medicine, University of Tromsø, Tromsø, Norway. elisabeth.jarhelle@unn.no.
Hansen GÅM; Northern Norway Family Cancer Center, Department of Medical Genetics, University Hospital of North Norway, Tromsø, Norway. elisabeth.jarhelle@unn.no.
Skarsfjord S; Department of Medical Genetics, Division of Child and Adolescent Health, University Hospital of North Norway, Tromsø, Norway.
Jonsrud C; Northern Norway Family Cancer Center, Department of Medical Genetics, University Hospital of North Norway, Tromsø, Norway.
Ingebrigtsen M; Department of Medical Genetics, Division of Child and Adolescent Health, University Hospital of North Norway, Tromsø, Norway.
Strømsvik N; Northern Norway Family Cancer Center, Department of Medical Genetics, University Hospital of North Norway, Tromsø, Norway.
Van Ghelue M; Department of Medical Genetics, Division of Child and Adolescent Health, University Hospital of North Norway, Tromsø, Norway.

Sci Rep ; 9(1): 19986, 2019 12 27.

Article en En | MEDLINE | ID: mdl-31882575

Asunto(s)

Proteína BRCA1/genética; Proteína BRCA2/genética; Predisposición Genética a la Enfermedad; Mutación de Línea Germinal; Síndrome de Cáncer de Mama y Ovario Hereditario/genética; Adulto; Anciano; Anciano de 80 o más Años; Alelos; Sustitución de Aminoácidos; Biomarcadores de Tumor; Femenino; Estudios de Asociación Genética; Genotipo; Síndrome de Cáncer de Mama y Ovario Hereditario/diagnóstico; Humanos; Persona de Mediana Edad; Linaje; Polimorfismo de Nucleótido Simple

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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Mutación de Línea Germinal / Proteína BRCA1 / Predisposición Genética a la Enfermedad / Proteína BRCA2 / Síndrome de Cáncer de Mama y Ovario Hereditario Tipo de estudio: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Aged / Aged80 / Female / Humans / Middle aged Idioma: En Revista: Sci Rep Año: 2019 Tipo del documento: Article País de afiliación: Noruega

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