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Mutations in MED12 Cause X-Linked Ohdo Syndrome
Anneke T. Vulto-van Silfhout, Bert B.A. de Vries, Bregje W.M. van Bon, Alexander Hoischen, Martina Ruiterkamp-Versteeg, Christian Gilissen, Fangjian Gao, Marloes van Zwam, Cornelis L. Harteveld, Anthonie J. van Essen, Ben C.J. Hamel, Tjitske Kleefstra,
Michèl A.A.P. Willemsen, Helger G. Yntema, Hans van Bokhoven, Han G. Brunner, Thomas G. Boyer, Arjan P.M. de Brouwer
The American Journal of Human Genetics Volume 92, Issue 3, Pages 401-406 (March 2013)
DOI: 10.1016/j.ajhg.2013.01.007
Copyright © 2013 The American Society of Human Genetics Terms and Conditions
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The American Journal of Human Genetics 2013 92, 401-406DOI: (10.1016/j.ajhg.2013.01.007) Copyright © 2013 The American Society of Human Genetics Terms and Conditions
Figure 2
The American Journal of Human Genetics 2013 92, 401-406DOI: (10.1016/j.ajhg.2013.01.007) Copyright © 2013 The American Society of Human Genetics Terms and Conditions
