Individuals with 22q11.2 deletion syndrome (22q11.2DS) are impaired at exploring visual information in space; however, not much is known about visual form discrimination in the syndrome. Thirty-five individuals with 22q11.2DS and 41 controls completed a form discrimination task with global forms made up of local elements. Affected individuals demonstrated clear impairment in detecting local, but not global, differences. Nevertheless, 22q11.2DS participants easily discriminated the same local elements when they were displayed in isolation, and further use of a prime demonstrated preserved facilitation of local processing in 22q11.2DS. These results did not differ by age or IQ. This study illustrates the impact of visuospatial impairments on ...
Background: 22q11.2 deletion syndrome (22qDS) is a common microdeletion disorder arising from a dele...
In this article the general and specific cognitive impairments of the boy R.H. with a de novo deleti...
Carriers of the rare 22q11.2 microdeletion present with a high percentage of positive and negative s...
Individuals with chromosome 22q11.2 deletion syndrome (22q11.2DS) have been shown to have impairment...
BACKGROUND: People with 22q11.2 deletion syndrome (22q11DS) have difficulty processing social inform...
ObjectivesOur ability to generate mental representation of magnitude from sensory information affect...
Previous research demonstrates that people with 22q11.2 deletion syndrome (22q11DS) have social and ...
Children affected by the 22q11.2 deletion syndrome (22q11.2DS) have a specific neuropsychological pr...
One of the defining cognitive characteristics of the chromosome 22q deletion syndrome (DS22q11.2) is...
Individuals with 22q11.2 deletion syndrome (22q11DS) exhibit deficits in visuo-spatial reasoning, in...
The influence of visuo-spatial skills on numerical magnitude processing is the subject of a long-sta...
Abstract Background Previous research links social difficulties to atypical face exploration in 22q1...
Abstract Background Chromosome 22q11.2 Deletion Syndrome (22q11.2DS) occurs in approximately 1:4,000...
Abstract Background Chromosome 22q11.2 deletion syndrome (22q11.2DS) results from a 1.5- to 3-megaba...
Chromosome 22q11.2 microdeletion syndrome (22q11.2DS) is a genetic syndrome characterised by a uniqu...
Background: 22q11.2 deletion syndrome (22qDS) is a common microdeletion disorder arising from a dele...
In this article the general and specific cognitive impairments of the boy R.H. with a de novo deleti...
Carriers of the rare 22q11.2 microdeletion present with a high percentage of positive and negative s...
Individuals with chromosome 22q11.2 deletion syndrome (22q11.2DS) have been shown to have impairment...
BACKGROUND: People with 22q11.2 deletion syndrome (22q11DS) have difficulty processing social inform...
ObjectivesOur ability to generate mental representation of magnitude from sensory information affect...
Previous research demonstrates that people with 22q11.2 deletion syndrome (22q11DS) have social and ...
Children affected by the 22q11.2 deletion syndrome (22q11.2DS) have a specific neuropsychological pr...
One of the defining cognitive characteristics of the chromosome 22q deletion syndrome (DS22q11.2) is...
Individuals with 22q11.2 deletion syndrome (22q11DS) exhibit deficits in visuo-spatial reasoning, in...
The influence of visuo-spatial skills on numerical magnitude processing is the subject of a long-sta...
Abstract Background Previous research links social difficulties to atypical face exploration in 22q1...
Abstract Background Chromosome 22q11.2 Deletion Syndrome (22q11.2DS) occurs in approximately 1:4,000...
Abstract Background Chromosome 22q11.2 deletion syndrome (22q11.2DS) results from a 1.5- to 3-megaba...
Chromosome 22q11.2 microdeletion syndrome (22q11.2DS) is a genetic syndrome characterised by a uniqu...
Background: 22q11.2 deletion syndrome (22qDS) is a common microdeletion disorder arising from a dele...
In this article the general and specific cognitive impairments of the boy R.H. with a de novo deleti...
Carriers of the rare 22q11.2 microdeletion present with a high percentage of positive and negative s...