AbstractThe paper by Meyer-Lindenberg and colleagues in this issue of Neuron provides strong evidence that the absence of one or more genes in Williams syndrome leads to highly circumscribed pathology in the dorsal visual stream. This program of research demonstrates that neurocognitive architecture follows the same principles in typical and atypical development
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...
3As a genetic experiment of nature, Williams syndrome (WMS) is expressed on multiple biological leve...
AbstractThe paper by Meyer-Lindenberg and colleagues in this issue of Neuron provides strong evidenc...
AbstractA unique opportunity to understand genetic determinants of cognition is offered by Williams ...
AbstractA unique opportunity to understand genetic determinants of cognition is offered by Williams ...
Williams syndrome (WS) is a contiguous gene syndrome caused by hemizygous deletion of approximately ...
Williams syndrome (WS) is a contiguous gene syndrome caused by hemizygous deletion of approximately ...
contributed equally to this work. Williams syndrome (WS) is a rare neurodevelopmental disorder cause...
Visual information is believed to be processed through two distinct, yet interacting cortical stream...
Williams' syndrome (WS) is a rare, genetically based disorder of cognitive development. Affected ind...
Williams' syndrome (WS) is a rare, genetically based disorder of cognitive development. Affected ind...
BACKGROUND: Williams syndrome (WS) is a rare neurodevelopmental disorder arising from a hemizygotic ...
BACKGROUND: Williams syndrome (WS) is a rare neurodevelopmental disorder arising from a hemizygotic ...
Williams syndrome is a genetic neurodevelopmental disorder characterized by an uncommon hypersociabi...
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...
3As a genetic experiment of nature, Williams syndrome (WMS) is expressed on multiple biological leve...
AbstractThe paper by Meyer-Lindenberg and colleagues in this issue of Neuron provides strong evidenc...
AbstractA unique opportunity to understand genetic determinants of cognition is offered by Williams ...
AbstractA unique opportunity to understand genetic determinants of cognition is offered by Williams ...
Williams syndrome (WS) is a contiguous gene syndrome caused by hemizygous deletion of approximately ...
Williams syndrome (WS) is a contiguous gene syndrome caused by hemizygous deletion of approximately ...
contributed equally to this work. Williams syndrome (WS) is a rare neurodevelopmental disorder cause...
Visual information is believed to be processed through two distinct, yet interacting cortical stream...
Williams' syndrome (WS) is a rare, genetically based disorder of cognitive development. Affected ind...
Williams' syndrome (WS) is a rare, genetically based disorder of cognitive development. Affected ind...
BACKGROUND: Williams syndrome (WS) is a rare neurodevelopmental disorder arising from a hemizygotic ...
BACKGROUND: Williams syndrome (WS) is a rare neurodevelopmental disorder arising from a hemizygotic ...
Williams syndrome is a genetic neurodevelopmental disorder characterized by an uncommon hypersociabi...
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...
3As a genetic experiment of nature, Williams syndrome (WMS) is expressed on multiple biological leve...
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