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.

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Title:	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.
Author(s):	Leeuw, N. de ; Pfundt, R.P. ; Koolen, D.A. ; Neefs, I.; Scheltinga, I.; Mieloo, H.; Sistermans, E.A. ; Nillesen, W.M.; Smeets, D.F.C.M. ; Vries, L.B.A. de ; Knoers, N.V.A.M.
Publication year:	2008
Source:	Journal of Medical Genetics, vol. 45, iss. 2, (2008), pp. 122-124
ISSN:	0022-2593
DOI:	https://doi.org/10.1136/jmg.2007.054049
Publication type:	Article / Letter to editor
Please use this identifier to cite or link to this item : http://hdl.handle.net/2066/69185
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Subject:	DCN 2: Functional Neurogenomics IGMD 3: Genomic disorders and inherited multi-system disorders IGMD 5: Health aging / healthy living IGMD 9: Renal disorder NCMLS 5: Membrane transport and intracellular motility UMCN 3.2: Cognitive neurosciences UMCN 5.1: Genetic defects of metabolism
Organization:	Human Genetics
Journal title:	Journal of Medical Genetics
Volume:	vol. 45
Issue:	iss. 2
Page start:	p. 122
Page end:	p. 124

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