Velocardiofacial syndrome (VCFS), also known as 22q11.2 deletion syndrome, is a neurogenetic disorder that is associated with both learning disabilities and a consistent neuropsychological phenotype, including deficits in executive function, visuospatial perception, and working memory. Anatomic imaging studies have identified significant volumetric reductions in the parietal lobe of individuals with VCFS, but several studies have reported that the frontal lobe is relatively preserved. We used functional magnetic resonance imaging to investigate the neural correlates of non-spatial working memory in 17 youths with VCFS, 10 of their unaffected siblings, and 10 community controls (with the same proportion of learning disabilities as the VCFS y...
22q11.2 deletion syndrome (22q11DS) is a genetic disorder associated with a microdeletion of chromos...
BackgroundChromosome 22q11.2 deletion syndrome is one of the most common genetic causes of cognitive...
Caused by a microdeletion at the q11.2 locus of chromosome 22, velo-cardio-facial syndrome (also kno...
Ninety-two children with velocardiofacial syndrome (VCFS), a genetic disorder caused by a microdelet...
Background: Velo-cardio-facial syndrome (VCFS, MIM#192430, 22q11.2 Deletion Syndrome) is a genetic d...
Abstract Background Velo-cardio-facial syndrome (VCFS, MIM#192430, 22q11.2 Deletion Syndrome) is a g...
Objective: Velo-cardio-facial syndrome (VCFS; 22q11.2 deletion syndrome) represents one of the highe...
Impairments in executive function, such as working memory, are almost universal in children with chr...
Some previous studies showed that verbal short-term memory (STM) is better preserved than visuospati...
Background: Children with chromosome 22q11.2 deletion syndrome (22q11.2DS) exhibit nonverbal learnin...
22q11.2 deletion syndrome (22q11DS) is a genetic disorder associated with a microdeletion of chromos...
BackgroundNeurofibromatosis Type 1 (NF1) is a genetic disorder that disrupts central nervous system ...
Background: Velo-cardio-facial syndrome (VCFS, 22q11.2 deletion) is characterized by severely delaye...
BACKGROUND: As children with velocardiofacial syndrome (VCFS) develop, they are at increased risk fo...
International audience22q11.2 deletion syndrome (22q11DS), also known as velo-cardio-facial syndrome...
22q11.2 deletion syndrome (22q11DS) is a genetic disorder associated with a microdeletion of chromos...
BackgroundChromosome 22q11.2 deletion syndrome is one of the most common genetic causes of cognitive...
Caused by a microdeletion at the q11.2 locus of chromosome 22, velo-cardio-facial syndrome (also kno...
Ninety-two children with velocardiofacial syndrome (VCFS), a genetic disorder caused by a microdelet...
Background: Velo-cardio-facial syndrome (VCFS, MIM#192430, 22q11.2 Deletion Syndrome) is a genetic d...
Abstract Background Velo-cardio-facial syndrome (VCFS, MIM#192430, 22q11.2 Deletion Syndrome) is a g...
Objective: Velo-cardio-facial syndrome (VCFS; 22q11.2 deletion syndrome) represents one of the highe...
Impairments in executive function, such as working memory, are almost universal in children with chr...
Some previous studies showed that verbal short-term memory (STM) is better preserved than visuospati...
Background: Children with chromosome 22q11.2 deletion syndrome (22q11.2DS) exhibit nonverbal learnin...
22q11.2 deletion syndrome (22q11DS) is a genetic disorder associated with a microdeletion of chromos...
BackgroundNeurofibromatosis Type 1 (NF1) is a genetic disorder that disrupts central nervous system ...
Background: Velo-cardio-facial syndrome (VCFS, 22q11.2 deletion) is characterized by severely delaye...
BACKGROUND: As children with velocardiofacial syndrome (VCFS) develop, they are at increased risk fo...
International audience22q11.2 deletion syndrome (22q11DS), also known as velo-cardio-facial syndrome...
22q11.2 deletion syndrome (22q11DS) is a genetic disorder associated with a microdeletion of chromos...
BackgroundChromosome 22q11.2 deletion syndrome is one of the most common genetic causes of cognitive...
Caused by a microdeletion at the q11.2 locus of chromosome 22, velo-cardio-facial syndrome (also kno...