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Browsing by Author Greef, J.C. de

Full Text	Issue Date	Title	Author(s)
	2011	Mutations in ZBTB24 are associated with immunodeficiency, centromeric instability, and facial anomalies syndrome type 2	Greef, J.C. de; Wang, J.; Balog, J.; Dunnen, J.T. den; Frants, R.R., et al
	2010	Clinical features of facioscapulohumeral muscular dystrophy 2.	Greef, J.C. de; Lemmers, R.J.; Camano, P.; Day, J.W.; Sacconi, S., et al
	2009	Common epigenetic changes of D4Z4 in contraction-dependent and contraction-independent FSHD.	Greef, J.C. de; Lemmers, R.J.; Engelen, B.G.M. van; Sacconi, S.; Venance, S.L., et al
	2009	Contraction-dependent (FSHD1) and independent (FSHD2) epigenetic changes of D4Z4 unify FSHD.	Greef, J.C. de; Lemmers, R.J.L.F.; Engelen, B.G.M. van; Sacconi, S.; Venance, S.L., et al
	2008	Clinical spectrum of immunodeficiency, centromeric instability and facial dysmorphism (ICF syndrome).	Hagleitner, M.M.; Lankester, A.; Maraschio, P.; Hulten, M.; Fryns, J.P., et al
	2007	ICF syndrome: high variability of the chromosomal phenotype and association with classical Hodgkin lymphoma.	Schuetz, C.; Barbi, G.; Barth, T.F.; Hoenig, M.; Schulz, A., et al
	2007	Hypomethylation is restricted to the D4Z4 repeat array in phenotypic FSHD.	Greef, J.C. de; Wohlgemuth, M.; Chan, O.A.; Hansson, K.B.; Smeets, D.F.C.M., et al
	2006	No effect of folic acid and methionine supplementation on D4Z4 methylation in patients with facioscapulohumeral muscular dystrophy.	Kooi, E.L. van der; Greef, J.C. de; Wohlgemuth, M.; Frants, R.R.; Asseldonk, R.J. van, et al