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Germline heterozygous exons 8-11 pathogenic BARD1 gene deletion reported for the first time in a family with suspicion of a hereditary colorectal cancer syndrome: more than an incidental finding?
Carrera, Sergio; Rodríguez-Martínez, Ana Belén; Garin, Intza; Sarasola, Esther; Martínez, Cristina; Maortua, Hiart; Callejo, Almudena; Ruiz de Lobera, Abigail; Muñoz, Alberto; Miñambres, Nagore; Jiménez-Labaig, Pablo.
Afiliação
  • Carrera S; Hereditary Cancer Genetic Counseling Unit- Medical Oncology Department, Cruces University Hospital, Plaza de Cruces S/N. 48903, Baracaldo, Bizkaia, Spain. sergio.carrerarevilla@osakidetza.eus.
  • Rodríguez-Martínez AB; Molecular Genetics Laboratory, Basurto University Hospital, Bilbao, Spain.
  • Garin I; Molecular Genetics Laboratory, Cruces University Hospital, Baracaldo, Spain.
  • Sarasola E; Molecular Genetics Laboratory, Basurto University Hospital, Bilbao, Spain.
  • Martínez C; Molecular Genetics Laboratory, Cruces University Hospital, Baracaldo, Spain.
  • Maortua H; Molecular Genetics Laboratory, Cruces University Hospital, Baracaldo, Spain.
  • Callejo A; Medical Oncology Department, Cruces University Hospital, Baracaldo, Spain.
  • Ruiz de Lobera A; Medical Oncology Department, Cruces University Hospital, Baracaldo, Spain.
  • Muñoz A; Medical Oncology Department, Cruces University Hospital, Baracaldo, Spain.
  • Miñambres N; Medical Oncology Department, Cruces University Hospital, Baracaldo, Spain.
  • Jiménez-Labaig P; Medical Oncology Department, Cruces University Hospital, Baracaldo, Spain.
Hered Cancer Clin Pract ; 21(1): 2, 2023 Jan 28.
Article em En | MEDLINE | ID: mdl-36709314

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies Idioma: En Revista: Hered Cancer Clin Pract Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies Idioma: En Revista: Hered Cancer Clin Pract Ano de publicação: 2023 Tipo de documento: Article