Abstract Background Chromosome 22q11.2 deletion syndrome (22q11.2DS) results from a 1.5- to 3-megabase deletion on the long arm of chromosome 22 and occurs in approximately 1 in 4000 live births. Previous studies indicate that children with 22q11.2DS are impaired on tasks involving spatial attention. However, the degree to which these impairments are due to volitionally generated (endogenous) or reflexive (exogenous) orienting of attention is unclear. Additionally, the efficacy of these component attention processes throughout child development in 22q11.2DS has yet to be examined. Methods Here we compared the performance of a wide age range (7 to 14 years) of children with 22q11.2DS to typically developing (TD) children on a comprehensive v...
Chromosome 22q11.2 Deletion Syndrome (22q11.2DS) is caused by the most common human microdeletion, a...
Chromosome 22q11.2 Deletion Syndrome (22q11.2DS) is caused by the most common human microdeletion, a...
BackgroundChromosome 22q11.2 deletion syndrome (22q11.2DS), fragile X syndrome (FXS), and Turner syn...
Abstract Background Chromosome 22q11.2 deletion syndrome (22q11.2DS) results from a 1.5- to 3-megaba...
Abstract Background Chromosome 22q11.2 Deletion Syndrome (22q11.2DS) occurs in approximately 1:4,000...
One of the defining cognitive characteristics of the chromosome 22q deletion syndrome (DS22q11.2) is...
One of the defining cognitive characteristics of the chromosome 22q deletion syndrome (DS22q11.2) is...
Individuals with chromosome 22q11.2 deletion syndrome (22q11.2DS) have been shown to have impairment...
Individuals with chromosome 22q11.2 deletion syndrome (22q11.2DS) have been shown to have impairment...
Background: Chromosome 22q11.2 Deletion Syndrome (22q11.2DS) occurs in approximately 1:4,000 live bi...
Impairment in the executive control of attention has been found in youth with chromosome 22q11.2 del...
Impairment in the executive control of attention has been found in youth with chromosome 22q11.2 del...
Abstract Individuals with chromosome 22q11.2 deletion syndrome (22q11.2DS) have been shown to have i...
Chromosome 22q11.2 Deletion Syndrome (22q11.2DS) is caused by the most common human microdeletion, a...
Chromosome 22q11.2 Deletion Syndrome (22q11.2DS) is caused by the most common human microdeletion, a...
Chromosome 22q11.2 Deletion Syndrome (22q11.2DS) is caused by the most common human microdeletion, a...
Chromosome 22q11.2 Deletion Syndrome (22q11.2DS) is caused by the most common human microdeletion, a...
BackgroundChromosome 22q11.2 deletion syndrome (22q11.2DS), fragile X syndrome (FXS), and Turner syn...
Abstract Background Chromosome 22q11.2 deletion syndrome (22q11.2DS) results from a 1.5- to 3-megaba...
Abstract Background Chromosome 22q11.2 Deletion Syndrome (22q11.2DS) occurs in approximately 1:4,000...
One of the defining cognitive characteristics of the chromosome 22q deletion syndrome (DS22q11.2) is...
One of the defining cognitive characteristics of the chromosome 22q deletion syndrome (DS22q11.2) is...
Individuals with chromosome 22q11.2 deletion syndrome (22q11.2DS) have been shown to have impairment...
Individuals with chromosome 22q11.2 deletion syndrome (22q11.2DS) have been shown to have impairment...
Background: Chromosome 22q11.2 Deletion Syndrome (22q11.2DS) occurs in approximately 1:4,000 live bi...
Impairment in the executive control of attention has been found in youth with chromosome 22q11.2 del...
Impairment in the executive control of attention has been found in youth with chromosome 22q11.2 del...
Abstract Individuals with chromosome 22q11.2 deletion syndrome (22q11.2DS) have been shown to have i...
Chromosome 22q11.2 Deletion Syndrome (22q11.2DS) is caused by the most common human microdeletion, a...
Chromosome 22q11.2 Deletion Syndrome (22q11.2DS) is caused by the most common human microdeletion, a...
Chromosome 22q11.2 Deletion Syndrome (22q11.2DS) is caused by the most common human microdeletion, a...
Chromosome 22q11.2 Deletion Syndrome (22q11.2DS) is caused by the most common human microdeletion, a...
BackgroundChromosome 22q11.2 deletion syndrome (22q11.2DS), fragile X syndrome (FXS), and Turner syn...