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
Williams Syndrome (WS) is a rare neurodevelopmental disorder, approximately occurring 1 in 20 000 ...
Background\ud \ud Williams syndrome (WS) is a rare neurodevelopmental disorder arising from a hemizy...
Williams Syndrome (WS) is a genetic neurodevelopmental disorder caused by a submicroscopic deletion...
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 ...
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 ...
Visual information is believed to be processed through two distinct, yet interacting cortical stream...
Williams Syndrome (WS) is a rare neurodevelopmental disorder, approximately occurring 1 in 20 000 ...
3As a genetic experiment of nature, Williams syndrome (WMS) is expressed on multiple biological leve...
& The rare, genetically based disorder, Williams syndrome (WMS), produces a constellation of dis...
AbstractInteractions between environmental and genetic factors may contribute to neurodegenerative d...
Williams Syndrome (WS) is a rare neurodevelopmental disorder, approximately occurring 1 in 20 000 ...
Williams syndrome (WS) is a neurodevelopmental condition that commonly occurs as a result of a conti...
The uneven cognitive phenotype in the adult outcome of Williams syndrome has led some researchers to...
Williams Syndrome (WS) is a rare neurodevelopmental disorder, approximately occurring 1 in 20 000 ...
Background\ud \ud Williams syndrome (WS) is a rare neurodevelopmental disorder arising from a hemizy...
Williams Syndrome (WS) is a genetic neurodevelopmental disorder caused by a submicroscopic deletion...
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 ...
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 ...
Visual information is believed to be processed through two distinct, yet interacting cortical stream...
Williams Syndrome (WS) is a rare neurodevelopmental disorder, approximately occurring 1 in 20 000 ...
3As a genetic experiment of nature, Williams syndrome (WMS) is expressed on multiple biological leve...
& The rare, genetically based disorder, Williams syndrome (WMS), produces a constellation of dis...
AbstractInteractions between environmental and genetic factors may contribute to neurodegenerative d...
Williams Syndrome (WS) is a rare neurodevelopmental disorder, approximately occurring 1 in 20 000 ...
Williams syndrome (WS) is a neurodevelopmental condition that commonly occurs as a result of a conti...
The uneven cognitive phenotype in the adult outcome of Williams syndrome has led some researchers to...
Williams Syndrome (WS) is a rare neurodevelopmental disorder, approximately occurring 1 in 20 000 ...
Background\ud \ud Williams syndrome (WS) is a rare neurodevelopmental disorder arising from a hemizy...
Williams Syndrome (WS) is a genetic neurodevelopmental disorder caused by a submicroscopic deletion...
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