Prader-Willi Syndrome and psychotic symptoms: 1. Case descriptions and genetic studies
By: Clarke, D (et al).
Series: Journal of Intellectual Disability Research 46 (2) 2002: 451-454. 2002Content type: text Media type: unmediated Carrier type: volume Subject(s): CASE STUDIES | DUAL DIAGNOSIS | GENETICS | PRADER WILLI SYNDROMESummary: Genetic studies were possible in five cases and SNRPN expression was examined in three cases. Maternal unipartental disomy and 15q11q13 deletions were found, demonstrating that pyschotic symptoms are not associated with a single type of genetic abnormality. [AJ]Item type | Current library | Call number | Status | Date due | Barcode | Item holds | |
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Article Research | IHC Library | Article (Browse shelf(Opens below)) | Available (Article available on request) | 10787 |
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Genetic studies were possible in five cases and SNRPN expression was examined in three cases. Maternal unipartental disomy and 15q11q13 deletions were found, demonstrating that pyschotic symptoms are not associated with a single type of genetic abnormality. [AJ]
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