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Browsing by Author Tops, C.M.

Full Text	Issue Date	Title	Author(s)
	2011	Risk of colorectal and endometrial cancers in EPCAM deletion-positive Lynch syndrome: a cohort study	Kempers, M.J.E.; Kuiper, R.P.; Ockeloen, C.W.; Chappuis, P.O.; Hutter, P., et al
	2011	Recurrence and variability of germline EPCAM deletions in Lynch syndrome	Kuiper, R.P.; Vissers, L.E.L.M.; Venkatachalam, R.; Bodmer, D.; Hoenselaar, E., et al
	2010	SDHAF2 mutations in familial and sporadic paraganglioma and phaeochromocytoma.	Bayley, J.P.M.; Kunst, H.P.M.; Cascon, A.; Sampietro, M.L.; Gaal, J., et al
	2010	Quantification of sequence exchange events between PMS2 and PMS2CL provides a basis for improved mutation scanning of Lynch syndrome patients.	Klift, H.M. van der; Tops, C.M.; Bik, E.C.; Boogaard, M.W.; Borgstein, A.M., et al
	2009	Chromosome 8q23.3 and 11q23.1 variants modify colorectal cancer risk in Lynch syndrome.	Wijnen, J.T.; Brohet, R.M.; Eijk, R. van; Jagmohan-Changur, S.; Middeldorp, A., et al
	2007	Germline mutations in APC and MUTYH are responsible for the majority of families with attenuated familial adenomatous polyposis.	Nielsen, M.; Hes, F.J.; Nagengast, F.M.; Weiss, M.M.; Mathus-Vliegen, E.M.H., et al
	2006	MUTYH and the mismatch repair system: partners in crime?	Niessen, R.C.; Sijmons, R.H.; Ou, J.; Olthof, S.G.; Osinga, J., et al
	2005	Multiplicity in polyp count and extracolonic manifestations in 40 Dutch patients with MYH associated polyposis coli (MAP).	Nielsen, M.; Franken, P.F.; Reinards, T.H.; Weiss, M.M.; Wagner, A., et al