Williams syndrome (WS) is rare genetic form of mental retardation caused by a micro-deletion on chromosome 7q11.23 that causes cognitive impairment and a variety of physical abnormalities. MRI studies of WS have demonstrated a series of brain abnormalities, including decreased brain size, with a relatively greater decrease in the volume of the cerebral white matter volume as compared to the cerebral gray matter. Moreover there is evidence that the posterior cerebrum is more affected in that persons with WS have a greater ratio of frontal to posterior regional volume. These findings are further supported by automated analyses that have shown reduced gray matter density in the superior parietal lobe areas. Functional MRI studies have demonstr...
Williams syndrome (WS) is a neurogenetic disorder resulting from a hemizygous microdeletion at band ...
We describe the results of a functional and structural brain connectivity analysis comparing a homog...
We describe the results of a functional and structural brain connectivity analysis comparing a homog...
Background: We investigated structural brain morphology of intellectually disabled children with Wil...
AbstractA unique opportunity to understand genetic determinants of cognition is offered by Williams ...
Williams syndrome (WS) is a neurodevelopmental disorder associated with deletion of ∼20 contiguous g...
Background:Williams syndrome (WMS) is a rare, ge-netically based syndrome associated with a hemidele...
Williams syndrome (WS) is a contiguous gene syndrome caused by hemizygous deletion of approximately ...
Williams Syndrome (WS) is a rare genetic disorder with unique behavioral features. Yet the rareness ...
Williams syndrome (WS) is a contiguous gene syndrome caused by hemizygous deletion of approximately ...
We describe the results of a functional and structural brain connectivity analysis comparing a homog...
Understanding patterns of gyrification in neurogenetic disorders helps to uncover the neurodevelopme...
Several lines of investigation suggest that individuals with Williams syndrome (WS), a neurodevelopm...
Williams syndrome (WS) is a neurodevelopmental condition that commonly occurs as a result of a conti...
Several lines of investigation suggest that individuals with Williams syndrome (WS), a neurodevelopm...
Williams syndrome (WS) is a neurogenetic disorder resulting from a hemizygous microdeletion at band ...
We describe the results of a functional and structural brain connectivity analysis comparing a homog...
We describe the results of a functional and structural brain connectivity analysis comparing a homog...
Background: We investigated structural brain morphology of intellectually disabled children with Wil...
AbstractA unique opportunity to understand genetic determinants of cognition is offered by Williams ...
Williams syndrome (WS) is a neurodevelopmental disorder associated with deletion of ∼20 contiguous g...
Background:Williams syndrome (WMS) is a rare, ge-netically based syndrome associated with a hemidele...
Williams syndrome (WS) is a contiguous gene syndrome caused by hemizygous deletion of approximately ...
Williams Syndrome (WS) is a rare genetic disorder with unique behavioral features. Yet the rareness ...
Williams syndrome (WS) is a contiguous gene syndrome caused by hemizygous deletion of approximately ...
We describe the results of a functional and structural brain connectivity analysis comparing a homog...
Understanding patterns of gyrification in neurogenetic disorders helps to uncover the neurodevelopme...
Several lines of investigation suggest that individuals with Williams syndrome (WS), a neurodevelopm...
Williams syndrome (WS) is a neurodevelopmental condition that commonly occurs as a result of a conti...
Several lines of investigation suggest that individuals with Williams syndrome (WS), a neurodevelopm...
Williams syndrome (WS) is a neurogenetic disorder resulting from a hemizygous microdeletion at band ...
We describe the results of a functional and structural brain connectivity analysis comparing a homog...
We describe the results of a functional and structural brain connectivity analysis comparing a homog...