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Molecular Background of Colorectal Tumors From Patients With Lynch Syndrome Associated With Germline Variants in PMS2.
Ten Broeke, Sanne W; van Bavel, Tom C; Jansen, Anne M L; Gómez-García, Encarnca; Hes, Frederik J; van Hest, Liselot P; Letteboer, Tom G W; Olderode-Berends, Maran J W; Ruano, Dina; Spruijt, Liesbeth; Suerink, Manon; Tops, Carli M; van Eijk, Ronald; Morreau, Hans; van Wezel, Tom; Nielsen, Maartje.
Afiliação
  • Ten Broeke SW; Department of Clinical Genetics, Leiden University Medical Center, Leiden, the Netherlands. Electronic address: tenbroeke@lumc.nl.
  • van Bavel TC; Department of Clinical Genetics, Leiden University Medical Center, Leiden, the Netherlands.
  • Jansen AML; Department of Pathology, Leiden University Medical Center, Leiden, the Netherlands.
  • Gómez-García E; Department of Clinical Genetics, Maastricht University Medical Center, Maastricht, the Netherlands.
  • Hes FJ; Department of Clinical Genetics, Leiden University Medical Center, Leiden, the Netherlands.
  • van Hest LP; Department of Clinical Genetics, VU University Medical Center, Amsterdam, the Netherlands.
  • Letteboer TGW; Department of Clinical Genetics, University Medical Center Utrecht, Utrecht, the Netherlands.
  • Olderode-Berends MJW; Department of Clinical Genetics, University Medical Center Groningen, Groningen, the Netherlands.
  • Ruano D; Department of Pathology, Leiden University Medical Center, Leiden, the Netherlands.
  • Spruijt L; Department of Clinical Genetics, Radboud University Medical Center, Radboud, the Netherlands.
  • Suerink M; Department of Clinical Genetics, Leiden University Medical Center, Leiden, the Netherlands.
  • Tops CM; Department of Clinical Genetics, Leiden University Medical Center, Leiden, the Netherlands.
  • van Eijk R; Department of Pathology, Leiden University Medical Center, Leiden, the Netherlands.
  • Morreau H; Department of Pathology, Leiden University Medical Center, Leiden, the Netherlands.
  • van Wezel T; Department of Pathology, Leiden University Medical Center, Leiden, the Netherlands.
  • Nielsen M; Department of Clinical Genetics, Leiden University Medical Center, Leiden, the Netherlands.
Gastroenterology ; 155(3): 844-851, 2018 09.
Article em En | MEDLINE | ID: mdl-29758216

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Neoplasias Colorretais Hereditárias sem Polipose / Mutação em Linhagem Germinativa / Endonuclease PMS2 de Reparo de Erro de Pareamento Tipo de estudo: Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Gastroenterology Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Neoplasias Colorretais Hereditárias sem Polipose / Mutação em Linhagem Germinativa / Endonuclease PMS2 de Reparo de Erro de Pareamento Tipo de estudo: Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Gastroenterology Ano de publicação: 2018 Tipo de documento: Article
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