22q11 deletion syndrome: a review of the neuropsychiatric features and their neurobiological basis
Chiara Squarcione, Maria Chiara Torti, Fabio Di Fabio, Massimo Biondi Department of Neurology and Psychiatry, Sapienza University of Rome, Rome, Italy Abstract: The 22q11.2 deletion syndrome (22q11DS) is caused by an autosomal dominant microdeletion of chromosome 22 at the long arm (q) 11.2 band. Th...
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| Auteurs principaux: | , , , |
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| Format: | article |
| Langue: | EN |
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Dove Medical Press
2013
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| Accès en ligne: | https://doaj.org/article/65aac41b1b1c42f8baa7e755238c1fe7 |
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