Colorectal cancer risk variants at 8q23.3 and 11q23.1 are associated with disease phenotype in APC mutation carriers

Familial adenomatous polyposis (FAP) is a dominantly inherited syndrome caused by germline mutations in the APC gene and characterized by the development of multiple colorectal adenomas and a high risk of developing colorectal cancer (CRC). The severity of polyposis is correlated with the site of th...

Full description

Saved in:
Bibliographic Details
Published in:Fam Cancer
Main Authors: Ghorbanoghli, Z., Nieuwenhuis, M. H., Houwing-Duistermaat, J. J., Jagmohan-Changur, S., Hes, F. J., Tops, C. M., Wagner, A., Aalfs, C. M., Verhoef, S., Gómez García, E. B., Sijmons, R. H., Menko, F. H., Letteboer, T. G., Hoogerbrugge, N., van Wezel, T., Vasen, H. F. A., Wijnen, J. T.
Format: Artigo
Language:Inglês
Published: Springer Netherlands 2016
Subjects:
Original Article
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC5010832/
https://ncbi.nlm.nih.gov/pubmed/26880076
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10689-016-9877-5
Tags: Add Tag
No Tags, Be the first to tag this record!

Similar Items