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.
Publication year
2014Source
Case Reports in Genetics, 2014, (2014), pp. 530134ISSN
Publication type
Article / Letter to editor

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Organization
Human Genetics
Radboudumc Extern
Journal title
Case Reports in Genetics
Volume
vol. 2014
Page start
p. 530134
Subject
Radboudumc 7: Neurodevelopmental disorders DCMN: Donders Center for Medical Neuroscience; Radboudumc 7: Neurodevelopmental disorders RIMLS: Radboud Institute for Molecular Life SciencesThis item appears in the following Collection(s)
- Academic publications [229196]
- Electronic publications [111643]
- Faculty of Medical Sciences [87796]
- Open Access publications [80446]
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