Deletions in the 3' part of the NFIX gene including a recurrent Alu-mediated deletion of exon 6 and 7 account for previously unexplained cases of Marshall-Smith syndrome
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| Description | scientific article published on 8 July 2014 |
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author: Martin Zenker Valérie Cormier-Daire Denny Schanze André Reis Raoul Hennekam |
| Publication date | July 8, 2014 |
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