A Rare, Recurrent, De Novo 14q32.2q32.31 Microdeletion of 1.1 Mb in a 20-Year-Old Female Patient with a Maternal UPD(14)-Like Phenotype and Intellectual Disability.

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Title:	A Rare, Recurrent, De Novo 14q32.2q32.31 Microdeletion of 1.1 Mb in a 20-Year-Old Female Patient with a Maternal UPD(14)-Like Phenotype and Intellectual Disability.
Author(s):	Zada, A.; Mundhofir, F.E.P. ; Pfundt, R.P. ; Leijsten, N.; Nillesen, W.; Faradz, S.M.H. ; Leeuw, N. de
Publication year:	2014
Source:	Case Reports in Genetics, vol. 2014, (2014), pp. 530134
ISSN:	2090-6544
DOI:	https://doi.org/10.1155/2014/530134
Publication type:	Article / Letter to editor
Please use this identifier to cite or link to this item : https://hdl.handle.net/2066/137136
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Subject:	Radboudumc 7: Neurodevelopmental disorders DCMN: Donders Center for Medical Neuroscience Radboudumc 7: Neurodevelopmental disorders RIMLS: Radboud Institute for Molecular Life Sciences
Organization:	Human Genetics Radboudumc Extern
Journal title:	Case Reports in Genetics
Volume:	vol. 2014
Page start:	p. 530134

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