Add to ORKGAbstract: 22q11.2 deletion syndrome (22q11.2DS) is a well-known genetic risk factor for schizophrenia. The catechol-O-methyltransferase (COMT) gene falls within the 22q11.2 minimal critical region of the deletion. Brain activity, as measured by functional magnetic resonance imaging (fMRI) during a Go/NoGo, response inhibition task was assessed in adolescents with 22q11.2DS (n 13), typically developing (TD) controls (n 14), and controls with developmental disability (DD, n 9). Subjects with 22q11.2DS were also genotyped for the COMTMet/Val polymorphism. Groups did not differ on task performance. However, compared to both control groups, the 22q11.2DS group showed greater brain activation within left parietal regions. Comparison of brain a...
22q11.2 deletion syndrome (22q11DS) is a genetic disorder associated with a microdeletion of chromos...
22q11.2 deletion syndrome (22q11DS) is caused by a microdeletion on chromosome 22q11.2 and associate...
The 22q11.2 deletion (22q11DS) is a common chromosomal microdeletion and a potent risk factor for ps...
22q11.2 deletion syndrome (22q11.2DS) is a well-known genetic risk factor for schizophrenia. The cat...
22q11.2 Deletion syndrome (22q11DS) is the most common known recurrent copy-number variant disorder....
Chromosome 22q11.2 deletion syndrome (22q11.2DS) is a neurogenetic disorder that is associated with ...
The 22q11.2 deletion is one of the most common copy number variants in humans. Carriers of the delet...
Although schizophrenia is strongly hereditary, there are limited data regarding biological risk fact...
22q11.2 deletion syndrome (22q11DS) is a neurogenetic disorder that causes a high risk of developing...
Chromosome 22q11.2 deletion syndrome (22q11DS) is a common microdeletion syndrome associated with a ...
22q11.2 deletion syndrome (22q11DS) is a genetic syndrome associated with a microdeletion of the chr...
The 22q11.2 deletion (22q11DS) is a common chromosomal microdeletion and a potent risk factor for ps...
22q11.2 Deletion Syndrome (22q11DS) is the most common genetic microdeletion syndrome affect-ing hum...
22q11.2 deletion syndrome (22q11DS) is associated with an increased susceptibility to develop schizo...
The 22q11.2 deletion (22q11DS) is a common chromosomal microdeletion and a potent risk factor for ps...
22q11.2 deletion syndrome (22q11DS) is a genetic disorder associated with a microdeletion of chromos...
22q11.2 deletion syndrome (22q11DS) is caused by a microdeletion on chromosome 22q11.2 and associate...
The 22q11.2 deletion (22q11DS) is a common chromosomal microdeletion and a potent risk factor for ps...
22q11.2 deletion syndrome (22q11.2DS) is a well-known genetic risk factor for schizophrenia. The cat...
22q11.2 Deletion syndrome (22q11DS) is the most common known recurrent copy-number variant disorder....
Chromosome 22q11.2 deletion syndrome (22q11.2DS) is a neurogenetic disorder that is associated with ...
The 22q11.2 deletion is one of the most common copy number variants in humans. Carriers of the delet...
Although schizophrenia is strongly hereditary, there are limited data regarding biological risk fact...
22q11.2 deletion syndrome (22q11DS) is a neurogenetic disorder that causes a high risk of developing...
Chromosome 22q11.2 deletion syndrome (22q11DS) is a common microdeletion syndrome associated with a ...
22q11.2 deletion syndrome (22q11DS) is a genetic syndrome associated with a microdeletion of the chr...
The 22q11.2 deletion (22q11DS) is a common chromosomal microdeletion and a potent risk factor for ps...
22q11.2 Deletion Syndrome (22q11DS) is the most common genetic microdeletion syndrome affect-ing hum...
22q11.2 deletion syndrome (22q11DS) is associated with an increased susceptibility to develop schizo...
The 22q11.2 deletion (22q11DS) is a common chromosomal microdeletion and a potent risk factor for ps...
22q11.2 deletion syndrome (22q11DS) is a genetic disorder associated with a microdeletion of chromos...
22q11.2 deletion syndrome (22q11DS) is caused by a microdeletion on chromosome 22q11.2 and associate...
The 22q11.2 deletion (22q11DS) is a common chromosomal microdeletion and a potent risk factor for ps...