22q11.2 Deletion Syndrome is associated with cognitive, behavioural, and psychiatric problems and is known to affect brain structure. Recently, 22q11.2 Deletion Syndrome has been proposed as a disease model for a genetic subtype of schizophrenia. In this paper we discuss the currently available literature on neurocognitive functioning and brain anatomy in patients with 22q11.2 Deletion Syndrome, and how this contributes to our understanding of the neurobiology of schizophrenia. Research on cognitive functioning in 22q11.2 Deletion Syndrome patients suggests a specific cognitive profile with impairments on arithmetical, visuo-spatial, and executive tasks and relatively preserved language skills. Prominent findings of neuroimaging studies in ...
22q11.2 deletion syndrome (22q11.2DS) is a neurogenetic condition associated with increased risk for...
The 22q11.2 deletion (22q11DS) is a common chromosomal microdeletion and a potent risk factor for ps...
Background and Purpose—The 22q11.2 deletion syndrome is a common genetic microdeletion syndrome that...
22q11.2 Deletion Syndrome is associated with cognitive, behavioural, and psychiatric problems and is...
The 22q11.2 deletion is one of the most common copy number variants in humans. Carriers of the delet...
22q11.2 Deletion syndrome (22q11DS) is the most common known recurrent copy-number variant disorder....
Adults with 22q11.2 Deletion syndrome (22q11DS) have increased prevalence of schizophrenia features....
22q11.2 deletion syndrome (22q11DS) is a neurogenetic disorder that causes a high risk of developing...
22q11.2 Deletion Syndrome (22q11DS) is the most common genetic microdeletion syndrome affect-ing hum...
Approximately 30% of individuals with 22q11.2 Deletion Syndrome (22q11DS) develop schizophrenia duri...
Introduction. 22q11.2 Deletion Syndrome (22q11.2DS; MIM #192430, MIM #188400) is the most common rec...
Investigators at Bambino Genu Children's Hospital, Rome, and multiple additional centers in Italy co...
Background: Chromosome 22q11.2 deletion syndrome (22q11.2DS) is a neurogenetic disorder that is asso...
22q11.2 deletion syndrome is characterised by a well defined microdeletion that is associated with a...
22q11.2 deletion syndrome (22q11DS) is a recurrent genetic mutation that is highly penetrant for psy...
22q11.2 deletion syndrome (22q11.2DS) is a neurogenetic condition associated with increased risk for...
The 22q11.2 deletion (22q11DS) is a common chromosomal microdeletion and a potent risk factor for ps...
Background and Purpose—The 22q11.2 deletion syndrome is a common genetic microdeletion syndrome that...
22q11.2 Deletion Syndrome is associated with cognitive, behavioural, and psychiatric problems and is...
The 22q11.2 deletion is one of the most common copy number variants in humans. Carriers of the delet...
22q11.2 Deletion syndrome (22q11DS) is the most common known recurrent copy-number variant disorder....
Adults with 22q11.2 Deletion syndrome (22q11DS) have increased prevalence of schizophrenia features....
22q11.2 deletion syndrome (22q11DS) is a neurogenetic disorder that causes a high risk of developing...
22q11.2 Deletion Syndrome (22q11DS) is the most common genetic microdeletion syndrome affect-ing hum...
Approximately 30% of individuals with 22q11.2 Deletion Syndrome (22q11DS) develop schizophrenia duri...
Introduction. 22q11.2 Deletion Syndrome (22q11.2DS; MIM #192430, MIM #188400) is the most common rec...
Investigators at Bambino Genu Children's Hospital, Rome, and multiple additional centers in Italy co...
Background: Chromosome 22q11.2 deletion syndrome (22q11.2DS) is a neurogenetic disorder that is asso...
22q11.2 deletion syndrome is characterised by a well defined microdeletion that is associated with a...
22q11.2 deletion syndrome (22q11DS) is a recurrent genetic mutation that is highly penetrant for psy...
22q11.2 deletion syndrome (22q11.2DS) is a neurogenetic condition associated with increased risk for...
The 22q11.2 deletion (22q11DS) is a common chromosomal microdeletion and a potent risk factor for ps...
Background and Purpose—The 22q11.2 deletion syndrome is a common genetic microdeletion syndrome that...