Contribution of bi-allelic germline MUTYH mutations to early-onset and familial colorectal cancer and to low number of adenomatous polyps: case-series and literature review

Autor: B. Jorritsma, Helga Westers, Renee C. Niessen, Carli M. J. Tops, H. J. van Kranen, Rolf H. Sijmons, C. L. E. Siezen, J. Varkevisser, Frederik J. Hes, Juul T. Wijnen, Alain Knopperts, R. C. Heine-Broring, Ellen Kampman, Maartje Nielsen, Yvonne J. Vos

Publikováno v: Familial Cancer, 12(1), 43-50
Familial Cancer, 12, 43-50
Familial Cancer, 12(1), 43-50. SPRINGER
Familial Cancer, 12, 1, pp. 43-50
Familial Cancer 12 (2013) 1

Item does not contain fulltext In the absence of a polyposis phenotype, colorectal cancer (CRC) patients referred for genetic testing because of early-onset disease and/or a positive family history, typically undergo testing for molecular signs of Ly

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https://research.wur.nl/en/publications/contribution-of-bi-allelic-germline-mutyh-mutations-to-early-onse