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Perceived burden and neuropsychiatric morbidities in adults with 22q11.2 deletion syndrome

BACKGROUND: 22q11.2 deletion syndrome (22q11.2DS) is a common genetic subtype of intellectual disability (ID) remarkable for its constellation of congenital, developmental and later-onset features. Survival to adulthood is now the norm, and serious psychiatric illness is common in adults. However, l...

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Bibliografske podrobnosti
izdano v:J Intellect Disabil Res
Main Authors: Karas, D. J., Costain, G., Chow, E. W. C., Bassett, A. S.
Format: Artigo
Jezik:Inglês
Izdano: 2012
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC4516411/
https://ncbi.nlm.nih.gov/pubmed/23106770
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1365-2788.2012.01639.x
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