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Browsing by Author Peeters, E.A.

Full Text	Issue Date	Title	Author(s)
	2012	Presence of ATM protein and residual kinase activity correlates with the phenotype in ataxia-telangiectasia: a genotype-phenotype study.	Verhagen, M.M.M.; Last, J.I.; Hogervorst, F.B.L.; Smeets, D.F.C.M.; Roeleveld, N., et al
	2012	Mutations in SWI/SNF chromatin remodeling complex gene ARID1B cause Coffin-Siris syndrome	Santen, G.W.; Aten, E.; Sun, Y; Almomani, R.; Gilissen, C.F., et al
	2012	Mutations in ISPD cause Walker-Warburg syndrome and defective glycosylation of alpha-dystroglycan	Roscioli, T.; Kamsteeg, E.J.; Buysse, K.; Maystadt, I.; Reeuwijk, J. van, et al
	2012	Incidence of acquired demyelinating syndromes of the CNS in Dutch children: a nationwide study.	Ketelslegers, I.A.; Catsman-Berrevoets, C.E.; Neuteboom, R.F.; Boon, M.; Dijk, K.G., 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