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Mutations in MED12 Cause X-Linked Ohdo Syndrome

✍ Scribed by Vulto-van Silfhout, Anneke T.; de Vries, Bert B.A.; van Bon, Bregje W.M.; Hoischen, Alexander; Ruiterkamp-Versteeg, Martina; Gilissen, Christian; Gao, Fangjian; van Zwam, Marloes; Harteveld, Cornelis L.; van Essen, Anthonie J.; Hamel, Ben C.J.; Kleefstra, Tjitske; Willemsen, Michèl A.A.P.; Yntema, Helger G.; van Bokhoven, Hans; Brunner, Han G.; Boyer, Thomas G.; de Brouwer, Arjan P.M.


Book ID
118742079
Publisher
American Society of Human Genetics
Year
2013
Tongue
English
Weight
538 KB
Volume
92
Category
Article
ISSN
0002-9297

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