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Combined mismatch repair and POLE/POLD1 defects explain unresolved suspected Lynch syndrome cancers.
Jansen, Anne Ml; van Wezel, Tom; van den Akker, Brendy Ewm; Ventayol Garcia, Marina; Ruano, Dina; Tops, Carli Mj; Wagner, Anja; Letteboer, Tom Gw; Gómez-García, Encarna B; Devilee, Peter; Wijnen, Juul T; Hes, Frederik J; Morreau, Hans.
Afiliação
  • Jansen AM; Department of Pathology, Leiden University Medical Centre, Leiden, The Netherlands.
  • van Wezel T; Department of Human Genetics, Leiden University Medical Centre, Leiden, The Netherlands.
  • van den Akker BE; Department of Pathology, Leiden University Medical Centre, Leiden, The Netherlands.
  • Ventayol Garcia M; Department of Pathology, Leiden University Medical Centre, Leiden, The Netherlands.
  • Ruano D; Department of Pathology, Leiden University Medical Centre, Leiden, The Netherlands.
  • Tops CM; Department of Pathology, Leiden University Medical Centre, Leiden, The Netherlands.
  • Wagner A; Department of Clinical 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.
  • Devilee P; Department of Clinical Genetics, University Hospital Maastricht, Maastricht, The Netherlands.
  • Wijnen JT; Department of Human Genetics, 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.
Eur J Hum Genet ; 24(7): 1089-92, 2016 07.
Article em En | MEDLINE | ID: mdl-26648449
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais Hereditárias sem Polipose / DNA Polimerase II / DNA Polimerase III / Reparo de Erro de Pareamento de DNA Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Eur J Hum Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Holanda País de publicação: Reino Unido
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais Hereditárias sem Polipose / DNA Polimerase II / DNA Polimerase III / Reparo de Erro de Pareamento de DNA Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Eur J Hum Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Holanda País de publicação: Reino Unido