Mutations in ANKRD11 cause KBG syndrome, characterized by intellectual disability, skeletal malformations, and macrodontia
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| Description | scientific article |
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author: Bruno Dallapiccola Emanuele Agolini Stephan Züchner Francesco Brancati Güney Bademci Mustafa Tekin |
| Publication date | August 12, 2011 |
| Language | English |
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| Missing/wrong data? | Edit Wikidata item |