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Case Reports in Genetics
Volume 2014, Article ID 530134, 5 pages
http://dx.doi.org/10.1155/2014/530134
Case Report

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

1Department of Human Genetics, Radboud University Medical Center, The Netherlands Division of Human Genetics, P.O. Box 9101, 6500 HB Nijmegen, The Netherlands
2Center for Biomedical Research (CEBIOR), Faculty of Medicine, Diponegoro University, GSG 2nd Floor, Jl. Dr. Sutomo 14, Semarang 50244, Indonesia

Received 27 December 2013; Accepted 19 February 2014; Published 30 March 2014

Academic Editors: C. López Ginés and G. Perez de Nanclares

Copyright © 2014 Almira Zada et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

How to Cite this Article

Almira Zada, Farmaditya E. P. Mundhofir, Rolph Pfundt, et al., “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,” Case Reports in Genetics, vol. 2014, Article ID 530134, 5 pages, 2014. https://doi.org/10.1155/2014/530134.