22q11 deletion syndrome: a review of the neuropsychiatric features and their neurobiological basis

The 22q11.2 deletion syndrome (22q11DS) is caused by an autosomal dominant microdeletion of chromosome 22 at the long arm (q) 11.2 band. The 22q11DS is among the most clinically variable syndromes, with more than 180 features related with the deletion, and is associated with an increased risk of psy...

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Detalles Bibliográficos
Autores principales: Squarcione, Chiara, Torti, Maria Chiara, Di Fabio, Fabio, Biondi, Massimo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2013
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3862513/
https://www.ncbi.nlm.nih.gov/pubmed/24353423
http://dx.doi.org/10.2147/NDT.S52188

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