Williams syndrome (WS) is a rare genetic disorder with a unique cognitive profile in which verbal abilities are markedly stronger than visuospatial abilities. This study investigated the claim that orientation coding is a specific deficit within the visuospatial domain in WS. Experiment 1 employed a simplified version of the Benton Judgement of Line Orientation task and a control, length-matching task. Results demonstrated comparable levels of orientation matching performance in the group with WS and a group of typically developing (TD) controls matched by nonverbal ability, although it is possible that floor effects masked group differences. A group difference was observed in the length-matching task due to stronger performance from the co...
Individuals with Williams syndrome typically show relatively poor visuo-spatial abilities in compari...
Individuals with Williams syndrome typically show relatively poor visuospatial abilities in comparis...
Williams syndrome (WS) is a neurodevelopmental disorder of known genetic origin. A characteristicall...
Williams syndrome (WS) is a rare genetic disorder with a unique cognitive profile in which verbal ab...
Williams syndrome (WS) is a rare genetic disorder with a unique cognitive profile in which verbal ab...
The visuo-spatial perceptual abilities of individuals with Williams syndrome (WS) were investigated ...
Individuals with Williams syndrome (WS) display poor visuo-spatial cognition relative to verbal abil...
Individuals with Williams syndrome (WS) display poor visuo-spatial cognition relative to verbal abil...
The visuo-spatial abilities of individuals with Williams syndrome (WS) have consistently been shown ...
The visuo-spatial abilities of individuals with Williams syndrome (WS) have consistently been shown ...
The visuospatial perceptual abilities of individuals with Williams syndrome (WS) were investigated i...
Individuals with Williams syndrome (WS) demonstrate impaired visuo-spatial abilities in comparison t...
Williams syndrome (WS) is a rare genetic disorder. At a cognitive level, this population display poo...
Individuals with Williams syndrome (WS) demonstrate impaired visuo-spatial abilities in comparison t...
Williams syndrome (WS) is a rare genetic disorder. At a cognitive level, this population display poo...
Individuals with Williams syndrome typically show relatively poor visuo-spatial abilities in compari...
Individuals with Williams syndrome typically show relatively poor visuospatial abilities in comparis...
Williams syndrome (WS) is a neurodevelopmental disorder of known genetic origin. A characteristicall...
Williams syndrome (WS) is a rare genetic disorder with a unique cognitive profile in which verbal ab...
Williams syndrome (WS) is a rare genetic disorder with a unique cognitive profile in which verbal ab...
The visuo-spatial perceptual abilities of individuals with Williams syndrome (WS) were investigated ...
Individuals with Williams syndrome (WS) display poor visuo-spatial cognition relative to verbal abil...
Individuals with Williams syndrome (WS) display poor visuo-spatial cognition relative to verbal abil...
The visuo-spatial abilities of individuals with Williams syndrome (WS) have consistently been shown ...
The visuo-spatial abilities of individuals with Williams syndrome (WS) have consistently been shown ...
The visuospatial perceptual abilities of individuals with Williams syndrome (WS) were investigated i...
Individuals with Williams syndrome (WS) demonstrate impaired visuo-spatial abilities in comparison t...
Williams syndrome (WS) is a rare genetic disorder. At a cognitive level, this population display poo...
Individuals with Williams syndrome (WS) demonstrate impaired visuo-spatial abilities in comparison t...
Williams syndrome (WS) is a rare genetic disorder. At a cognitive level, this population display poo...
Individuals with Williams syndrome typically show relatively poor visuo-spatial abilities in compari...
Individuals with Williams syndrome typically show relatively poor visuospatial abilities in comparis...
Williams syndrome (WS) is a neurodevelopmental disorder of known genetic origin. A characteristicall...