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Case Reports in Genetics
Volume 2012, Article ID 949507, 3 pages
http://dx.doi.org/10.1155/2012/949507
Case Report

Mowat-Wilson Syndrome: The First Clinical and Molecular Report of an Indonesian Patient

Farmaditya E. P. Mundhofir,1,2 Helger G. Yntema,2 Ineke van der Burgt,2 Ben C. J. Hamel,2 Sultana M. H. Faradz,1 and Bregje W. M. van Bon2

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

Received 20 October 2012; Accepted 6 November 2012

Academic Editors: S. Chappell, R. Perry, and M. Suri

Copyright © 2012 Farmaditya E. P. Mundhofir 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

Farmaditya E. P. Mundhofir, Helger G. Yntema, Ineke van der Burgt, Ben C. J. Hamel, Sultana M. H. Faradz, and Bregje W. M. van Bon, “Mowat-Wilson Syndrome: The First Clinical and Molecular Report of an Indonesian Patient,” Case Reports in Genetics, vol. 2012, Article ID 949507, 3 pages, 2012. https://doi.org/10.1155/2012/949507.