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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...
Wedi'i Gadw mewn:
| Cyhoeddwyd yn: | J Intellect Disabil Res |
|---|---|
| Prif Awduron: | , , , |
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
2012
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| Pynciau: | |
| Mynediad Ar-lein: | 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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