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Cognitive, Behavioural and Psychiatric Phenotype in 22q11.2 Deletion Syndrome
22q11.2 Deletion syndrome has become an important model for understanding the pathophysiology of neurodevelopmental conditions, particularly schizophrenia which develops in about 20–25% of individuals with a chromosome 22q11.2 microdeletion. From the initial discovery of the syndrome, associated dev...
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| Hlavní autoři: | , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2011
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3139630/ https://ncbi.nlm.nih.gov/pubmed/21573985 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10519-011-9468-z |
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