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Browsing by Author Wessels, M.W.

Full Text	Issue Date	Title	Author(s)
	2011	Mutations in SMAD3 cause a syndromic form of aortic aneurysms and dissections with early-onset osteoarthritis	Laar, I.M. van de; Oldenburg, R.A.; Pals, G.; Roos-Hesselink, J.W.; Graaf, B.M. de, et al
	2010	Mucopolysaccharidosis type IIID: 12 new patients and 15 novel mutations.	Valstar, M.J.; Bertoli-Avella, A.M.; Wessels, M.W.; Ruijter, G.J.; Graaf, B. de, et al
	2009	Autosomal dominant inheritance of cardiac valves anomalies in two families: extended spectrum of left-ventricular outflow tract obstruction.	Wessels, M.W.; Laar, I.M. van de; Roos-Hesselink, J.W.; Strikwerda, S.; Majoor-Krakauer, D.F., et al
	2008	A new syndrome with noncompaction cardiomyopathy, bradycardia, pulmonary stenosis, atrial septal defect and heterotaxy with suggestive linkage to chromosome 6p.	Wessels, M.W.; Graaf, B.M. de; Cohen-Overbeek, T.E.; Spitaels, S.E.; Laat, L.E. de Groot-de, et al
	2005	Autosomal dominant inheritance of left ventricular outflow tract obstruction.	Wessels, M.W.; Berger, R.M.; Frohn-Mulder, I.M.; Roos-Hesselink, J.W.; Hoogeboom, J.J., et al
	2004	Three new families with arterial tortuosity syndrome.	Wessels, M.W.; Catsman-Berrevoets, C.E.; Mancini, G.M.; Breuning, M.H.; Hoogeboom, J.J., et al