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BRCA1 and BRCA2 genetic testing-pitfalls and recommendations for managing variants of uncertain clinical significance.
Eccles, D M; Mitchell, G; Monteiro, A N A; Schmutzler, R; Couch, F J; Spurdle, A B; Gómez-García, E B.
Afiliação
  • Eccles DM; Faculty of Medicine Academic Unit of Cancer Sciences, Southampton General Hospital, Southampton, UK.
  • Mitchell G; Familial Cancer Centre, Peter MacCallum Cancer Centre, The University of Melbourne, Melbourne, Australia Hereditary Cancer Program, Department of Medical Oncology, University of British Columbia, Vancouver, Canada.
  • Monteiro AN; Cancer Epidemiology Program, H. Lee Moffitt Cancer Center, Tampa, USA.
  • Schmutzler R; Center for Hereditary Breast and Ovarian Cancer, Center for Integrated Oncology (CIO) and Center for Molecular Medicine Cologne (CMMC), University Hospital Cologne, Cologne, Germany.
  • Couch FJ; Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, USA.
  • Spurdle AB; Molecular Cancer Epidemiology Laboratory, Division of Genetics and Computational Biology, QIMR Berghofer Medical Research Institute, BNE, Herston, Australia.
  • Gómez-García EB; Department of Clinical Genetics, Maastricht University Medical Centre, Maastricht, The Netherlands Encarna.Gomezgarcia@mumc.nl.
Ann Oncol ; 26(10): 2057-65, 2015 Oct.
Article em En | MEDLINE | ID: mdl-26153499
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Neoplasias Ovarianas / Variação Genética / Neoplasias da Mama / Testes Genéticos / Proteína BRCA1 / Proteína BRCA2 / Mutação Tipo de estudo: Etiology_studies / Guideline / Prognostic_studies / Risk_factors_studies Limite: Female / Humans Idioma: En Revista: Ann Oncol Assunto da revista: NEOPLASIAS Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Reino Unido
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Neoplasias Ovarianas / Variação Genética / Neoplasias da Mama / Testes Genéticos / Proteína BRCA1 / Proteína BRCA2 / Mutação Tipo de estudo: Etiology_studies / Guideline / Prognostic_studies / Risk_factors_studies Limite: Female / Humans Idioma: En Revista: Ann Oncol Assunto da revista: NEOPLASIAS Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Reino Unido