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The Schizophrenia Phenotype in 22q11 Deletion Syndrome
OBJECTIVE: This study investigated the schizophrenia phenotype in 24 subjects with 22q11 deletion syndrome (22qDS) and schizophrenia (22qDS-schizophrenia), a rare but relatively homogenous genetic subtype of schizophrenia associated with a microdeletion on chromosome 22. Individuals with 22qDS are a...
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| Asıl Yazarlar: | , , , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
2003
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3276594/ https://ncbi.nlm.nih.gov/pubmed/12944331 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1176/appi.ajp.160.9.1580 |
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