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Browsing by Author Mieloo, H.

Full Text	Issue Date	Title	Author(s)
	2010	Phenotypic spectrum of 20 novel patients with molecularly defined supernumerary marker chromosomes 15 and a review of the literature.	Kleefstra, T.; Leeuw, N. de; Wolf, R.; Nillesen, W.M.; Schobers, G., 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
	2008	A newly recognised microdeletion syndrome involving 2p15p16.1: narrowing down the critical region by adding another patient detected by genome wide tiling path array comparative genomic hybridisation analysis.	Leeuw, N. de; Pfundt, R.P.; Koolen, D.A.; Neefs, I.; Scheltinga, I., et al
	2007	Further refinement of the candidate region for monosomy 9p syndrome.	Faas, B.H.W.; Leeuw, N. de; Mieloo, H.; Bruinenberg, J.; Vries, B. de
	2006	Cryptic duplication of the distal segment of 22q due to a translocation (21;22): three case reports and a review of the literature.	Feenstra, I.; Koolen, D.A.; Pas, J. van der; Hamel, B.C.J.; Mieloo, H., et al