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Cerebral cortex three-dimensional profiling in human fetuses by magnetic resonance imaging

✍ Scribed by Andrea Sbarbati; Francesca Pizzini; Paolo F. Fabene; Elena Nicolato; Pasquina Marzola; Laura Calderan; Alessandro Simonati; Laura Longo; Antonio Osculati; Alberto Beltramello

Book ID
110729891
Publisher
John Wiley and Sons
Year
2004
Tongue
English
Weight
295 KB
Volume
204
Category
Article
ISSN
0021-8782

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## Abstract The neuropathologic abnormalities associated with Prader–Willi syndrome (PWS) are largely unknown. PWS is due to the loss of several paternally expressed genes in chromosome 15q11‐q13 region. Several of the imprinted genes in the 15q11‐q13 region are normally expressed in the brain and