Individuals with Williams syndrome (WS) demonstrate impaired visuo-spatial abilities in comparison to their level of verbal ability. In particular, visuo-spatial construction is an area of relative weakness. It has been hypothesised that poor or atypical location coding abilities contribute strongly to the impaired abilities observed on construction and drawing tasks [Farran, E. K., & Jarrold, C. (2005). Evidence for unusual spatial location coding in Williams syndrome: An explanation for the local bias in visuo-spatial construction tasks? Brain and Cognition, 59, 159–172; Hoffman, J. E., Landau, B., & Pagani, B. (2003). Spatial breakdown in spatial construction: Evidence from eye fixations in children with Williams syndrome. Cognitive Psyc...
Recent findings suggest that difficulties on small-scale visuospatial tasks documented in Williams s...
We investigated the role of executive and spatial representational processes in impaired per-formanc...
Williams syndrome (WS) is a rare genetic condition characterised by intellectual disability, typical...
Individuals with Williams syndrome (WS) demonstrate impaired visuo-spatial abilities in comparison t...
Individuals with Williams syndrome (WS) demonstrate impaired visuo-spatial abilities in comparison t...
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...
Williams syndrome (WS) is a neurodevelopmental disorder associated with an impaired capacity for vis...
main aim of this study was to test the claim that individuals with Williams syndrome have selectivel...
Williams syndrome (WS), a genetic deletion syndrome, is characterized by severe visuospatial deficit...
The visuo-spatial abilities of individuals with Williams syndrome (WS) have consistently been shown ...
Individuals with Williams syndrome typically show relatively poor visuo-spatial abilities in compari...
Williams syndrome (WS) is a genetic disorder associated with severe visuocognitive impairment. Indiv...
The visuo-spatial abilities of individuals with Williams syndrome (WS) have consistently been shown ...
Williams syndrome (WS) is a genetic disorder associated with severe visuocognitive impairment. Indiv...
Recent findings suggest that difficulties on small-scale visuospatial tasks documented in Williams s...
We investigated the role of executive and spatial representational processes in impaired per-formanc...
Williams syndrome (WS) is a rare genetic condition characterised by intellectual disability, typical...
Individuals with Williams syndrome (WS) demonstrate impaired visuo-spatial abilities in comparison t...
Individuals with Williams syndrome (WS) demonstrate impaired visuo-spatial abilities in comparison t...
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...
Williams syndrome (WS) is a neurodevelopmental disorder associated with an impaired capacity for vis...
main aim of this study was to test the claim that individuals with Williams syndrome have selectivel...
Williams syndrome (WS), a genetic deletion syndrome, is characterized by severe visuospatial deficit...
The visuo-spatial abilities of individuals with Williams syndrome (WS) have consistently been shown ...
Individuals with Williams syndrome typically show relatively poor visuo-spatial abilities in compari...
Williams syndrome (WS) is a genetic disorder associated with severe visuocognitive impairment. Indiv...
The visuo-spatial abilities of individuals with Williams syndrome (WS) have consistently been shown ...
Williams syndrome (WS) is a genetic disorder associated with severe visuocognitive impairment. Indiv...
Recent findings suggest that difficulties on small-scale visuospatial tasks documented in Williams s...
We investigated the role of executive and spatial representational processes in impaired per-formanc...
Williams syndrome (WS) is a rare genetic condition characterised by intellectual disability, typical...