Add to ORKGIn conclusion, this thesis includes findings from studies that support our hypothesis of abnormal neurotransmitter functioning in adults with 22q11DS as a consequence of reduced gene dosages, together with findings from studies that may help to improve challenge studies or diagnostic procedures in neuropsychiatric disorders. The findings presented in this thesis provide some insights in the complex relation between a genetic defect and (ab)normal brain function
22q11.2 Deletion syndrome (22q11DS) is the most common known recurrent copy-number variant disorder....
BACKGROUND: Individuals with 22q11.2 deletion syndrome (22q11DS) are at increased risk of developing...
Background: 22q11.2 deletion syndrome (22qDS) is a common microdeletion disorder arising from a dele...
22q11.2 deletion syndrome is characterised by a well defined microdeletion that is associated with a...
22q11 Deletion syndrome (22q11DS) is associated with chromosome 22q11 microdeletions and high rates ...
Patients with 22q11 deletion syndrome (22q11DS) have a high prevalence of psychiatric disorders and ...
22q11 Deletion syndrome (22q11DS) is a neurogenetic disorder, resulting from a hemizygous microdelet...
22q11.2 deletion syndrome (22q11DS), most frequently caused by a de novo microdeletion on the long a...
Evidence is rapidly accumulating that rare, recurrent copy number variants represent large effect ri...
Introduction. 22q11.2 Deletion Syndrome (22q11.2DS; MIM #192430, MIM #188400) is the most common rec...
It is now well recognized that as well as having a characteristic facial dysmorphology and a range o...
Although approximately 1 in 4 people is affected by mental disorders at some point in their lives, t...
22q11.2 Deletion Syndrome is associated with cognitive, behavioural, and psychiatric problems and is...
The etiology of Parkinson’s disease (PD) remains largely unknown with the exception of a few genetic...
The 22q11.2 deletion syndrome (22q11.2 DS) places affected individuals at an increased risk for neur...
22q11.2 Deletion syndrome (22q11DS) is the most common known recurrent copy-number variant disorder....
BACKGROUND: Individuals with 22q11.2 deletion syndrome (22q11DS) are at increased risk of developing...
Background: 22q11.2 deletion syndrome (22qDS) is a common microdeletion disorder arising from a dele...
22q11.2 deletion syndrome is characterised by a well defined microdeletion that is associated with a...
22q11 Deletion syndrome (22q11DS) is associated with chromosome 22q11 microdeletions and high rates ...
Patients with 22q11 deletion syndrome (22q11DS) have a high prevalence of psychiatric disorders and ...
22q11 Deletion syndrome (22q11DS) is a neurogenetic disorder, resulting from a hemizygous microdelet...
22q11.2 deletion syndrome (22q11DS), most frequently caused by a de novo microdeletion on the long a...
Evidence is rapidly accumulating that rare, recurrent copy number variants represent large effect ri...
Introduction. 22q11.2 Deletion Syndrome (22q11.2DS; MIM #192430, MIM #188400) is the most common rec...
It is now well recognized that as well as having a characteristic facial dysmorphology and a range o...
Although approximately 1 in 4 people is affected by mental disorders at some point in their lives, t...
22q11.2 Deletion Syndrome is associated with cognitive, behavioural, and psychiatric problems and is...
The etiology of Parkinson’s disease (PD) remains largely unknown with the exception of a few genetic...
The 22q11.2 deletion syndrome (22q11.2 DS) places affected individuals at an increased risk for neur...
22q11.2 Deletion syndrome (22q11DS) is the most common known recurrent copy-number variant disorder....
BACKGROUND: Individuals with 22q11.2 deletion syndrome (22q11DS) are at increased risk of developing...
Background: 22q11.2 deletion syndrome (22qDS) is a common microdeletion disorder arising from a dele...