Add to ORKGVelocardiofacial syndrome (VUS), the most frequent microdeletion syndrome identified in humans, is associated with chromosomal microdeletions in the q11 band of chromosome 22. Individuals with VCFS are reported to have a characteristic behavioral phenotype with high rates of behavioral, psychiatric, neuropsychological and linguistic disorders. It was noted that patients with VCFS have a higher prevalence of schizophrenia, mood disorders and attention deficit hyperactivity disorder. This article aimed to present a case of VCFS with schizophrenia. (Archives of Neuropsychiatry 2009; 46: 27-9
This is the first clinical description of a detailed psychological, speech, and language phenotype o...
This is the first clinical description of a detailed psychological, speech, and language phenotype o...
A man with intellectual disability presented with schizophrenia, hypocalcaemia, facial dysmorphism a...
Velocardiofacial syndrome (VCFS), the most frequent microdeletion syndrome identified in humans, is ...
BACKGROUND: Individuals with velocardio-facial syndrome (VCFS), a genetic disorder associated with m...
Among the many features with which velocardiofacial syndrome (VCFS) may present, we review in this p...
Velo-cardio-facial syndrome (VCFS) is a genetic disorder associated with 22q11 deletion, a character...
BACKGROUND: Velo-cardio-facial syndrome (VCFS), a syndrome characterized by an increased frequency...
Velocardiofacial syndrome (VCFS), also known as DiGeorge, conotruncal anomaly face, and Cayler syndr...
Objective: The aim of this paper is to report the diagnosis of velo-cardio-facial syndrome (VCFS) in...
BACKGROUND: As children with velocardiofacial syndrome (VCFS) develop, they are at increased risk fo...
BACKGROUND: Velo-cardio-facial syndrome (VCFS) is associated with interstitial deletions of chromoso...
Deletion of chr22q11 gives rise to velo-cardio facial syndrome (VCFS) and increases schizophrenia ri...
Velo-cardio-facial syndrome (vcfs) is a congenital disorder with a markedly variable clinical expres...
OBJECTIVE: Velocardiofacial syndrome (VCFS) is associated with cognitive deficits and high rates of ...
This is the first clinical description of a detailed psychological, speech, and language phenotype o...
This is the first clinical description of a detailed psychological, speech, and language phenotype o...
A man with intellectual disability presented with schizophrenia, hypocalcaemia, facial dysmorphism a...
Velocardiofacial syndrome (VCFS), the most frequent microdeletion syndrome identified in humans, is ...
BACKGROUND: Individuals with velocardio-facial syndrome (VCFS), a genetic disorder associated with m...
Among the many features with which velocardiofacial syndrome (VCFS) may present, we review in this p...
Velo-cardio-facial syndrome (VCFS) is a genetic disorder associated with 22q11 deletion, a character...
BACKGROUND: Velo-cardio-facial syndrome (VCFS), a syndrome characterized by an increased frequency...
Velocardiofacial syndrome (VCFS), also known as DiGeorge, conotruncal anomaly face, and Cayler syndr...
Objective: The aim of this paper is to report the diagnosis of velo-cardio-facial syndrome (VCFS) in...
BACKGROUND: As children with velocardiofacial syndrome (VCFS) develop, they are at increased risk fo...
BACKGROUND: Velo-cardio-facial syndrome (VCFS) is associated with interstitial deletions of chromoso...
Deletion of chr22q11 gives rise to velo-cardio facial syndrome (VCFS) and increases schizophrenia ri...
Velo-cardio-facial syndrome (vcfs) is a congenital disorder with a markedly variable clinical expres...
OBJECTIVE: Velocardiofacial syndrome (VCFS) is associated with cognitive deficits and high rates of ...
This is the first clinical description of a detailed psychological, speech, and language phenotype o...
This is the first clinical description of a detailed psychological, speech, and language phenotype o...
A man with intellectual disability presented with schizophrenia, hypocalcaemia, facial dysmorphism a...