| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5905020 | European Journal of Medical Genetics | 2012 | 6 Pages |
Abstract
⺠SETBP1 haploinsufficiency is related with expressive speech impairment. ⺠Array-CGH revealed a cryptic microdeletion in an apparently balanced translocation. ⺠SETBP1 analysis in patients with developmental delay, behavioural problems, verbal dyspraxia.
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Authors
Giuseppina Marseglia, Maria Rosaria Scordo, Chiara Pescucci, Genni Nannetti, Elisabetta Biagini, Valeria Scandurra, Francesca Gerundino, Alberto Magi, Matteo Benelli, Francesca Torricelli,