Psychogenetic Study in Patients with Prader-Willi Syndrome
Maha Hamed Moustafa;
Abstract
Prader–Willi syndrome (PWS) is a genetic disorder that results from the absence of normally active paternally expressed genes from the 15q11-q13 chromosome region. Approximately 70% of affected individuals have a deletion in this region; about 25% have
Other data
| Title | Psychogenetic Study in Patients with Prader-Willi Syndrome | Authors | Maha Hamed Moustafa | Keywords | Psychogenetic Study in Patients with Prader-Willi Syndrome | Issue Date | 2007 | Description | Prader–Willi syndrome (PWS) is a genetic disorder that results from the absence of normally active paternally expressed genes from the 15q11-q13 chromosome region. Approximately 70% of affected individuals have a deletion in this region; about 25% have |
Attached Files
| File | Size | Format | |
|---|---|---|---|
| 116755p7610.pdf | 8.74 MB | Adobe PDF | View/Open |
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