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CHEK2 c.1100delC mutation is associated with an increased risk for male breast cancer in Finnish patient population.
Hallamies, Sanna; Pelttari, Liisa M; Poikonen-Saksela, Paula; Jekunen, Antti; Jukkola-Vuorinen, Arja; Auvinen, Päivi; Blomqvist, Carl; Aittomäki, Kristiina; Mattson, Johanna; Nevanlinna, Heli.
Afiliación
  • Hallamies S; Department of Oncology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
  • Pelttari LM; Department of Obstetrics and Gynecology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
  • Poikonen-Saksela P; Department of Oncology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
  • Jekunen A; Vaasa Central Hospital, Oncologic Clinic, Turku University, Vaasa, Finland.
  • Jukkola-Vuorinen A; Department of Oncology and Radiotherapy, Medical Research Center Oulu, Oulu University Hospital and University of Oulu, Oulu, Finland.
  • Auvinen P; Department of Oncology, Kuopio University Hospital and Cancer Center, Institute of Clinical Medicine, University of Eastern Finland, Kuopio, Finland.
  • Blomqvist C; Department of Oncology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
  • Aittomäki K; Department of Clinical Genetics, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
  • Mattson J; Department of Oncology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
  • Nevanlinna H; Department of Obstetrics and Gynecology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland. heli.nevanlinna@hus.fi.
BMC Cancer ; 17(1): 620, 2017 Sep 05.
Article en En | MEDLINE | ID: mdl-28874143
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Eliminación de Secuencia / Neoplasias de la Mama Masculina / Predisposición Genética a la Enfermedad / Quinasa de Punto de Control 2 Tipo de estudio: Etiology_studies / Observational_studies / Risk_factors_studies / Screening_studies Límite: Adult / Aged / Aged80 / Humans / Male / Middle aged País/Región como asunto: Europa Idioma: En Revista: BMC Cancer Asunto de la revista: NEOPLASIAS Año: 2017 Tipo del documento: Article País de afiliación: Finlandia
Texto completo
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Eliminación de Secuencia / Neoplasias de la Mama Masculina / Predisposición Genética a la Enfermedad / Quinasa de Punto de Control 2 Tipo de estudio: Etiology_studies / Observational_studies / Risk_factors_studies / Screening_studies Límite: Adult / Aged / Aged80 / Humans / Male / Middle aged País/Región como asunto: Europa Idioma: En Revista: BMC Cancer Asunto de la revista: NEOPLASIAS Año: 2017 Tipo del documento: Article País de afiliación: Finlandia