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Whole Gene Capture Analysis of 15 CRC Susceptibility Genes in Suspected Lynch Syndrome Patients.
Jansen, Anne M L; Geilenkirchen, Marije A; van Wezel, Tom; Jagmohan-Changur, Shantie C; Ruano, Dina; van der Klift, Heleen M; van den Akker, Brendy E W M; Laros, Jeroen F J; van Galen, Michiel; Wagner, Anja; Letteboer, Tom G W; Gómez-García, Encarna B; Tops, Carli M J; Vasen, Hans F; Devilee, Peter; Hes, Frederik J; Morreau, Hans; Wijnen, Juul T.
Afiliação
  • Jansen AM; Department of Human Genetics, Leiden University Medical Centre, Leiden, The Netherlands.
  • Geilenkirchen MA; Department of Pathology, Leiden University Medical Centre, Leiden, The Netherlands.
  • van Wezel T; Department of Human Genetics, Leiden University Medical Centre, Leiden, The Netherlands.
  • Jagmohan-Changur SC; Department of Pathology, Leiden University Medical Centre, Leiden, The Netherlands.
  • Ruano D; Department of Human Genetics, Leiden University Medical Centre, Leiden, The Netherlands.
  • van der Klift HM; Department of Pathology, Leiden University Medical Centre, Leiden, The Netherlands.
  • van den Akker BE; Department of Human Genetics, Leiden University Medical Centre, Leiden, The Netherlands.
  • Laros JF; Department of Pathology, Leiden University Medical Centre, Leiden, The Netherlands.
  • van Galen M; Department of Human Genetics, Leiden University Medical Centre, Leiden, The Netherlands.
  • Wagner A; Department of Human Genetics, Leiden University Medical Centre, Leiden, The Netherlands.
  • Letteboer TG; Department of Clinical Genetics, Erasmus University Medical Centre, Rotterdam, The Netherlands.
  • Gómez-García EB; Department of Medical Genetics, University Medical Centre Utrecht, Utrecht, The Netherlands.
  • Tops CM; Department of Clinical Genetics, University Hospital Maastricht, Maastricht, The Netherlands.
  • Vasen HF; Department of Clinical Genetics, Leiden University Medical Centre, Leiden, The Netherlands.
  • Devilee P; Department of Gastroenterology and Hepatology, Leiden University Medical Centre, Leiden, The Netherlands.
  • Hes FJ; Department of Human Genetics, Leiden University Medical Centre, Leiden, The Netherlands.
  • Morreau H; Department of Clinical Genetics, Leiden University Medical Centre, Leiden, The Netherlands.
  • Wijnen JT; Department of Pathology, Leiden University Medical Centre, Leiden, The Netherlands.
PLoS One ; 11(6): e0157381, 2016.
Article em En | MEDLINE | ID: mdl-27300758
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Neoplasias Colorretais Hereditárias sem Polipose / Regulação Neoplásica da Expressão Gênica / Metilação de DNA / Reparo de Erro de Pareamento de DNA Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans / Middle aged Idioma: En Revista: PLoS One Assunto da revista: CIENCIA / MEDICINA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Holanda
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Neoplasias Colorretais Hereditárias sem Polipose / Regulação Neoplásica da Expressão Gênica / Metilação de DNA / Reparo de Erro de Pareamento de DNA Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans / Middle aged Idioma: En Revista: PLoS One Assunto da revista: CIENCIA / MEDICINA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Holanda