Interstitial 6q deletion with a Prader-Willi-like phenotype: a new case and review of the literature.

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Title:	Interstitial 6q deletion with a Prader-Willi-like phenotype: a new case and review of the literature.
Author(s):	Gilhuis, H.J.; Ravenswaaij-Arts, C.M.A. van ; Hamel, B.C.J. ; Gabreëls, F.J.M.
Publication year:	2000
Source:	EuropeanJOURNAL of Paediatric Neurology, vol. 4, (2000), pp. 39-43
ISSN:	1090-3798
Publication type:	Article / Letter to editor
Please use this identifier to cite or link to this item : http://hdl.handle.net/2066/150675
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Subject:	(Fragile) breakage-prone sites in human chromosomes Clinical description and delineation of genetic syndromes Pathophysiology of Brain and Behaviour Breuk-gevoelige plaatsen in chromosomen bij de mens Klinische beschrijving en moleculaire definiëring van genetische syndromen Pathofysiologie van Hersenen en Gedrag
Organization:	Neurology Human Genetics
Journal title:	European Journal of Paediatric Neurology
Volume:	vol. 4
Page start:	p. 39
Page end:	p. 43