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Browsing by Author Brussel, W.

Full Text	Issue Date	Title	Author(s)
	2011	A case of carotid artery dissection suggesting ADEM.	Walker, J.C.; Brussel, W.; Erasmus, C.E.
	2010	Deletions of the RUNX2 gene are present in about 10% of individuals with cleidocranial dysplasia.	Ott, C.E.; Leschik, G.; Trotier, F.; Brueton, L.; Brunner, H.G., et al
	2009	Guanidinoacetate methyltransferase (GAMT) deficiency diagnosed by proton NMR spectroscopy of body fluids.	Engelke, U.F.H.; Tassini, M.; Hayek, J.; Vries, M. de; Bilos, A., et al
	2008	tRNA splicing endonuclease mutations cause pontocerebellar hypoplasia.	Budde, B.S.; Namavar, Y.; Barth, P.G.; Poll-The, B.T.; Nurnberg, G., et al
	2004	Myo-inositol, glucose and zinc status as risk factors for non-syndromic cleft lip with or without cleft palate in offspring : a case-control study	Krapels, I.P.C.; Rooij, I.A.L.M. van; Wevers, R.A.; Zielhuis, G.A.; Spauwen, P.H.M., et al