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Browsing by Author Menko, F.H.

Full Text	Issue Date	Title	Author(s)
	2011	Hereditary leiomyomatosis and renal cell cancer in families referred for fumarate hydratase germline mutation analysis.	Smit, D.L.; Mensenkamp, A.R.; Badeloe, S.; Breuning, M.H.; Simon, M.E., et al
	2010	TP53 germline mutation testing in 180 families suspected of Li-Fraumeni syndrome: mutation detection rate and relative frequency of cancers in different familial phenotypes.	Ruijs, M.W.; Verhoef, S.; Rookus, M.A.; Pruntel, R.; Hout, A.H. van der, et al
	2010	Informing family members about a hereditary predisposition to cancer: attitudes and practices among clinical geneticists	Stol, Y.H.; Menko, F.H.; Westerman, M.J.; Janssens, R.
	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
	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
	2007	[DNA-based diagnosis of hereditary tumour predisposition]	Menko, F.H.; Ligtenberg, M.J.L.; Brouwer, T.; Hahn, D.E.; Ausems, M.G.E.M.
	2007	Is surveillance of the small bowel indicated for Lynch syndrome families?	Kate, G.L. ten; Kleibeuker, J.H.; Nagengast, F.M.; Craanen, M.; Cats, A., et al
	2005	Cancer risks in BRCA2 families: estimates for sites other than breast and ovary.	Asperen, C.J. van; Brohet, R.M.; Meijers-Heijboer, E.J.; Hoogerbrugge-van der Linden, N.; Verhoef, S., 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
	2004	Survival after adjuvant 5-FU treatment for stage III colon cancer in hereditary nonpolyposis colorectal cancer.	Vos tot Nederveen Cappel, W.H. de; Meulenbeld, H.J.; Kleibeuker, J.H.; Nagengast, F.M.; Menko, F.H., et al
	2004	The role of mismatch repair gene defects in the development of adenomas in patients with HNPCC.	Jong, A.E. de; Morreau, H.; Puijenbroek, M.; Eilers, P.H.; Wijnen, J.T., 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
	1996	A (G-to-A) mutation in the initiation codon of the proteolipid protein gene causing a relatively mild form of Pelizaeus-Merzbacher disease in a Dutch family	Sistermans, E.A.; Wijs, I.J. de; Coo, R.F.M. de; Smit, L.M.E.; Menko, F.H., et al
	1995	The gene for Hereditary Bullous dystrophy, X-linked Macular Type, maps to the Xq27.3-qter region	Wijker, M.; Ligtenberg, M.J.L.; Schoute, F.; Defesche, J.C.; Pals, G., et al
	1995	The Gene for Hereditary Bullous Dystrophy, X-Linked Macular Type, Maps to the Xq27.3-Qter Region	Wijker, M.; Ligtenberg, M.J.L.; Schoute, F.; Defesche, J.C.; Pals, G., et al