Colorectal cancer incidence in path_MLH1 carriers subjected to different follow-up protocols: a Prospective Lynch Syndrome Database report

Author(s):
Seppala, T.; Pylvanainen, K.; Evans, D.G.; Jarvinen, H.; Renkonen-Sinisalo, L.; Bernstein, I.; Holinski-Feder, E.; Sala, P.; Lindblom, A.; Macrae, F.; Blanco, I.; Sijmons, R.; Jeffries, J.; Vasen, H.; Burn, J.; Nakken, S.; Hovig, E.; Rodland, E.A.; Tharmaratnam, K.; Cappel, W.H.D.T.N.; Hill, J.; Wijnen, J.; Jenkins, M.; Genuardi, M.; Green, K.; Lalloo, F.; Sunde, L.; Mints, M.; Bertario, L.; Pineda, M.; Navarro, M.; Morak, M.; Frayling, I.M.; Plazzer, J.P.; Sampson, J.R.; Capella, G.; Moslein, G.; Mecklin, J.P.; Moller, P.; Collaboration Mallorca Grp
Published
2017
Publication type
Article / Letter to editor
Lynch syndromeHereditary non-polyposis colorectal cancerColorectal cancerMicrosatellite instability
Date issued
2017-10-10
Language
English
Is part of
Hereditary Cancer in Clinical Practice
hdl
1887/117538
doi
10.1186/s13053-017-0078-5