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Browsing by Author Gille, J.J.P.

Full Text	Issue Date	Title	Author(s)
	2012	Novel strategies in newborn screening for cystic fibrosis: a prospective controlled study.	Vernooij-van Langen, A.M.; Loeber, J.G.; Elvers, B.; Triepels, R.H.; Gille, J.J.P., et al
	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
	2009	A method to assess the clinical significance of unclassified variants in the BRCA1 and BRCA2 genes based on cancer family history.	Gomez Garcia, E.B.; Oosterwijk-Wakka, J.C.; Timmermans, M.; Asperen, C.J. van; Hogervorst, F.B.L., et al
	2009	A simple method for co-segregation analysis to evaluate the pathogenicity of unclassified variants; BRCA1 and BRCA2 as an example	Mohammadi, L.; Vreeswijk, M.P.; Oldenburg, R.; Ouweland, A.M.W. van den; Oosterwijk-Wakka, J.C., et al
	2008	Variable phenotypes associated with 10q23 microdeletions involving the PTEN and BMPR1A genes.	Menko, F.H.; Kneepkens, C.M.; Leeuw, N. de; Peeters, E.A.; Maldergem, L Van, et al
	1997	A high proportion of novel mutations in BRCA1 with strong founder effects among Dutch and Belgian hereditary breast and ovarian cancer families	Peelen, T.; Vliet, M. van; Petrij-Bosch, A.; Mieremet, R.; Szabo, C., et al