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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Publication year
2014
Author(s)
Zada, A.
Mundhofir, F.E.P.
Pfundt, R.P.
Leijsten, N.
Nillesen, W.
Faradz, S.M.H.
Leeuw, N. de
Source
Case Reports in Genetics, 2014, (2014), pp. 530134
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DOI
Publication type
Article / Letter to editor
Please use this identifier to cite or link to this item: https://hdl.handle.net/2066/137136   https://hdl.handle.net/2066/137136
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