SNP association study in PMS2-associated Lynch syndrome

Author:

ten Broeke Sanne W.,Elsayed Fadwa A.,Pagan Lisa,Olderode-Berends Maran J. W.,Garcia Encarna Gomez,Gille Hans J. P.,van Hest Liselot P.,Letteboer Tom G. W.,van der Kolk Lizet E.,Mensenkamp Arjen R.,van Os Theo A.,Spruijt Liesbeth,Redeker Bert J. W.,Suerink Manon,Vos Yvonne J.,Wagner Anja,Wijnen Juul T.,Steyerberg E. W.,Tops Carli M. J.,van Wezel Tom,Nielsen Maartje

Funder

KWF Kankerbestrijding

Publisher

Springer Science and Business Media LLC

Subject

Cancer Research,Genetics(clinical),Oncology,Genetics

Reference35 articles.

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3. ten Broeke SW, Brohet RM, Tops CM, van der Klift HM, Velthuizen ME, Bernstein I, Capella Munar G, Gomez Garcia E, Hoogerbrugge N, Letteboer TG, Menko FH, Lindblom A, Mensenkamp AR, Moller P, van Os TA, Rahner N, Redeker BJ, Sijmons RH, Spruijt L, Suerink M, Vos YJ, Wagner A, Hes FJ, Vasen HF, Nielsen M, Wijnen JT (2015) Lynch syndrome caused by germline PMS2 mutations: delineating the cancer risk. J Clin Oncol 33(4):319–325

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5. Wijnen JT, Brohet RM, van ER, Jagmohan-Changur S, Middeldorp A, Tops CM, PM van, MG Ausems, Gomez GE, Hes FJ, Hoogerbrugge N, Menko FH, van Os TA, Sijmons RH, Verhoef S, Wagner A, Nagengast FM, Kleibeuker JH, Devilee P, Morreau H, Goldgar D, Tomlinson IP, Houlston RS, Van WT, Vasen HF (2009) Chromosome 8 q23.3 and 11q23.1 variants modify colorectal cancer risk in Lynch syndrome. Gastroenterology 136(1):131–137

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