Your browser doesn't support javascript.
loading
Colorectal cancer risk variants at 8q23.3 and 11q23.1 are associated with disease phenotype in APC mutation carriers.
Ghorbanoghli, Z; Nieuwenhuis, M H; Houwing-Duistermaat, J J; Jagmohan-Changur, S; Hes, F J; Tops, C M; Wagner, A; Aalfs, C M; Verhoef, S; Gómez García, E B; Sijmons, R H; Menko, F H; Letteboer, T G; Hoogerbrugge, N; van Wezel, T; Vasen, H F A; Wijnen, J T.
Afiliação
  • Ghorbanoghli Z; Netherlands Foundation for the Detetion of Hereditary Tumors, Leiden, The Netherlands. z.ghorbanoghli@gmail.com.
  • Nieuwenhuis MH; Department of Gastroenterology and Hepatology, Leiden University Medical Centre, Rijnsburgerweg 10, 2333 AA, Leiden, The Netherlands. z.ghorbanoghli@gmail.com.
  • Houwing-Duistermaat JJ; Netherlands Foundation for the Detetion of Hereditary Tumors, Leiden, The Netherlands.
  • Jagmohan-Changur S; Department of Medical Statistics and Bioinformatics, Leiden University Medical Center, Leiden, The Netherlands.
  • Hes FJ; Department of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands.
  • Tops CM; Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.
  • Wagner A; Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.
  • Aalfs CM; Department of Clinical Genetics, Erasmus Medical Center, Rotterdam, The Netherlands.
  • Verhoef S; Department of Clinical Genetics, Amsterdam Medical Centre, Amsterdam, The Netherlands.
  • Gómez García EB; Family Cancer Clinic, the Netherlands Cancer Institute, Amsterdam, The Netherlands.
  • Sijmons RH; Department of Clinical Genetics, University of Maastricht, Maastricht, The Netherlands.
  • Menko FH; Department of Genetics, University Medical Centre Groningen, University of Groningen, Groningen, The Netherlands.
  • Letteboer TG; Department of Clinical Genetics, VU University Medical Center, Amsterdam, The Netherlands.
  • Hoogerbrugge N; Department of Medical Genetics, University Medical Centre Utrecht, Utrecht, The Netherlands.
  • van Wezel T; Department of Human Genetics, Radboud University Nijmegen Medical Center, Nijmegen, The Netherlands.
  • Vasen HF; Departments of Pathology, Leiden University Medical Center, Leiden, The Netherlands.
  • Wijnen JT; Netherlands Foundation for the Detetion of Hereditary Tumors, Leiden, The Netherlands.
Fam Cancer ; 15(4): 563-70, 2016 10.
Article em En | MEDLINE | ID: mdl-26880076
Assuntos
Palavras-chave
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 8 / Cromossomos Humanos Par 11 / Neoplasias Colorretais / Proteína da Polipose Adenomatosa do Colo Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Humans / Male Idioma: En Revista: Fam Cancer Assunto da revista: NEOPLASIAS Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Holanda
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 8 / Cromossomos Humanos Par 11 / Neoplasias Colorretais / Proteína da Polipose Adenomatosa do Colo Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Humans / Male Idioma: En Revista: Fam Cancer Assunto da revista: NEOPLASIAS Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Holanda