Crynodeb
Williams syndrome (WS) is a neurodevelopmental disorder associated with deletion of ∼ 20 contiguous genes in chromosome band 7q11.23. Individuals with WS exhibit mild to moderate mental retardation, but are relatively more proficient in specific language and musical abilities. We used tensor-based morphometry (TBM) to visualize the complex pattern of gray/white matter reductions in WS, based on fluid registration of structural brain images.
| Iaith wreiddiol | Saesneg |
|---|---|
| Tudalennau (o-i) | 1096-1109 |
| Nifer y tudalennau | 16 |
| Cyfnodolyn | Neuroimage |
| Cyfrol | 36 |
| Rhif cyhoeddi | 4 |
| Dynodwyr Gwrthrych Digidol (DOIs) | |
| Statws | Cyhoeddwyd - 2007 |