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Prevalence of the E318K and V320I MITF germline mutations in Polish cancer patients and multiorgan cancer risk-a population-based study.
Gromowski, Tomasz; Masojc, Bartlomiej; Scott, Rodney J; Cybulski, Cezary; Górski, Bohdan; Kluzniak, Wojciech; Paszkowska-Szczur, Katarzyna; Rozmiarek, Andrzej; Debniak, Boguslaw; Maleszka, Romuald; Kladny, Józef; Lubinski, Jan; Debniak, Tadeusz.
Afiliação
  • Gromowski T; Department of Genetics and Pathology, International Hereditary Cancer Center, Pomeranian Medical University, Szczecin, Poland. Electronic address: tomaszbiotech@gmail.com.
  • Masojc B; Department of Genetics and Pathology, International Hereditary Cancer Center, Pomeranian Medical University, Szczecin, Poland.
  • Scott RJ; Discipline of Medical Genetics, Faculty of Health, University of Newcastle and Hunter Medical Research Institute, Newcastle, NSW, Australia.
  • Cybulski C; Department of Genetics and Pathology, International Hereditary Cancer Center, Pomeranian Medical University, Szczecin, Poland.
  • Górski B; Department of Genetics and Pathology, International Hereditary Cancer Center, Pomeranian Medical University, Szczecin, Poland.
  • Kluzniak W; Department of Genetics and Pathology, International Hereditary Cancer Center, Pomeranian Medical University, Szczecin, Poland.
  • Paszkowska-Szczur K; Department of Genetics and Pathology, International Hereditary Cancer Center, Pomeranian Medical University, Szczecin, Poland.
  • Rozmiarek A; Regional Hospital, Zielona Góra, Poland.
  • Debniak B; Chair and Clinic of Mother's and Child's Health, Medical University, Poznan, Poland.
  • Maleszka R; Department of Dermatology and Venereology, Pomeranian Medical University, Szczecin, Poland.
  • Kladny J; Department of General and Oncological Surgery, Pomeranian Medical University, Szczecin, Poland.
  • Lubinski J; Department of Genetics and Pathology, International Hereditary Cancer Center, Pomeranian Medical University, Szczecin, Poland.
  • Debniak T; Department of Genetics and Pathology, International Hereditary Cancer Center, Pomeranian Medical University, Szczecin, Poland.
Cancer Genet ; 207(4): 128-32, 2014 Apr.
Article em En | MEDLINE | ID: mdl-24767713

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Mutação em Linhagem Germinativa / Mutação de Sentido Incorreto / Fator de Transcrição Associado à Microftalmia / Neoplasias Tipo de estudo: Etiology_studies / Prevalence_studies / Risk_factors_studies / Screening_studies Limite: Aged / Female / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Revista: Cancer Genet Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Mutação em Linhagem Germinativa / Mutação de Sentido Incorreto / Fator de Transcrição Associado à Microftalmia / Neoplasias Tipo de estudo: Etiology_studies / Prevalence_studies / Risk_factors_studies / Screening_studies Limite: Aged / Female / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Revista: Cancer Genet Ano de publicação: 2014 Tipo de documento: Article