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Mutations in MED12 cause X-linked Ohdo syndrome. [electronic resource] 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
Producer: 20130729
In:
American journal of human genetics vol. 92
Availability: No items available.
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