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Browsing by Author Aalfs, C.M.

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
	2011	Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriers.	Cox, D.G.; Simard, J.; Sinnett, D.; Hamdi, Y.; Soucy, P., et al
	2011	Evaluation of the XRCC1 gene as a phenotypic modifier in BRCA1/2 mutation carriers. Results from the consortium of investigators of modifiers of BRCA1/BRCA2	Osorio, A.; Milne, R.L.; Alonso, R.; Pita, G.; Peterlongo, P., et al
	2011	Interplay between BRCA1 and RHAMM Regulates Epithelial Apicobasal Polarization and May Influence Risk of Breast Cancer	Maxwell, C.A.; Benitez, J.; Gomez-Baldo, L.; Osorio, A.; Bonifaci, N., 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
	2010	Common breast cancer susceptibility alleles and the risk of breast cancer for BRCA1 and BRCA2 mutation carriers: implications for risk prediction.	Antoniou, A.C.; Beesley, J.; McGuffog, L.; Sinilnikova, O.M.; Healey, S., 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	Physical activity and the risk of breast cancer in BRCA1/2 mutation carriers.	Pijpe, A.; Manders, P.; Brohet, R.M.; Collee, J.M.; Verhoef, S., et al
	2009	Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers.	Antoniou, A.C.; Sinilnikova, O.M.; McGuffog, L.; Healey, S.; Nevanlinna, H., 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
	1997	Het Smith-Lemli-Opitz syndroom: een stoornis in de cholesterol biosynthese	Jira, P.E.; Jong, J.G.N. de; Metz, M. de; Aalfs, C.M.; Hennekam, R.C.M., et al
	1997	Het Smith Lemli Opitz syndroom: een stoornis in de cholesterol biosynthese	Jira, P.E.; Jong, J.G.N. de; Metz, M. de; Aalfs, C.M.; Hennekam, R.C.M., et al
	1995	Ziekte van Wilson; ontmaskering met behulp van kernspinresonantie-tomografie	Berg, J.S.P. van den; Hoogenraad, T.U.; Duyn, J.A.; Verbeeten, B.; Aalfs, C.M., et al