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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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Detaylı Bibliyografya
Asıl Yazarlar: Bassett, Anne S., Chow, Eva W.C., AbdelMalik, Philip, Gheorghiu, Mirona, Husted, Janice, Weksberg, Rosanna
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2003
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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