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Browsing by Author Ockeloen, C.W.

Full Text	Issue Date	Title	Author(s)
	2012	Oral application of bacterial lysate in infancy decreases the risk of atopic dermatitis in children with 1 atopic parent in a randomized, placebo-controlled trial	Lau, S.; Gerhold, K.; Zimmermann, K.; Ockeloen, C.W.; Rossberg, S., et al
	2012	Duplications of BHLHA9 are associated with ectrodactyly and tibia hemimelia inherited in non-Mendelian fashion	Klopocki, E.; Lohan, S.; Doelken, S.; Stricker, S.; Ockeloen, C.W., et al
	2012	Congenital myopathy caused by a novel missense mutation in the CFL2 gene.	Ockeloen, C.W.; Gilhuis, H.J.; Pfundt, R.; Kamsteeg, E.J.; Agrawal, P.B., 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	Two adjacent microdeletions in 8q11.2 cause a phenotype suggestive of the 22q11 deletion syndrome.	Ockeloen, C.W.; Leeuw, N. de; Mieloo, H.; Reijnen, I.G.; Vries, L.B.A. de