Background: Velocardiofacial syndrome (VCFS) is a congenital malformation syndrome with an estimated prevalence of 1:4,000 livebirths. Most cases are caused by a common 3 Mb deletion at 22q11.2. This syndrome exhibits wide inter- and intra-familial variability in phenotypic features including physical, developmental, neurological, and neuropsychiatric manifestations despite the general uniformity in deletion size. The purpose of this meta-analysis was to seek explanations for the differences in the reported prevalence rates of various findings; to more accurately estimate the prevalence of each of the nine traits examined; to provide insight into future research; and to improve the ability for genetic counselors and clinicians to provide mo...
Objective—Velo-cardio-facial syndrome (VCFS) is caused by a microdeletion of approximately 40 genes ...
Purpose of review: The understanding of velo-cardio-facial syndrome has grown markedly since the ini...
The extent to which the phenotype of children comorbid for velocardiofacial syndrome (VCFS) and auti...
Background: Velocardiofacial syndrome (VCFS) is a congenital malformation syndrome with an estimated...
Objective: The velocardiofacial syndrome (VCFS) involves a deletion of part of chromosome 22 and is ...
Velocardiofacial syndrome (VCFS) is one of the most common genetic disorders that affect every major...
OBJECTIVES: 22q11.2 deletion syndrome (22q11.2DS), also known as velocardiofacial syndrome (VCFS) or...
Velocardiofacial syndrome (VCFS), also known as DiGeorge, conotruncal anomaly face, and Cayler syndr...
Item does not contain fulltextThe velo-cardio-facial syndrome (VCFS) is a leading cause of velophary...
BACKGROUND: As children with velocardiofacial syndrome (VCFS) develop, they are at increased risk fo...
In this contribution the current status and recent findings of the behavioural phenotype in VCFS (22...
Among the many features with which velocardiofacial syndrome (VCFS) may present, we review in this p...
Velocardiofacial syndrome, also called Shprintzen syndrome or DiGeorge sequence, is one of the most ...
Background Velocardiofacial syndrome (VCFS) is a microdeletion syndrome caused by a 22q11.2 chromoso...
In this contribution the current status and recent findings of the behavioural phenotype in VCFS (22...
Objective—Velo-cardio-facial syndrome (VCFS) is caused by a microdeletion of approximately 40 genes ...
Purpose of review: The understanding of velo-cardio-facial syndrome has grown markedly since the ini...
The extent to which the phenotype of children comorbid for velocardiofacial syndrome (VCFS) and auti...
Background: Velocardiofacial syndrome (VCFS) is a congenital malformation syndrome with an estimated...
Objective: The velocardiofacial syndrome (VCFS) involves a deletion of part of chromosome 22 and is ...
Velocardiofacial syndrome (VCFS) is one of the most common genetic disorders that affect every major...
OBJECTIVES: 22q11.2 deletion syndrome (22q11.2DS), also known as velocardiofacial syndrome (VCFS) or...
Velocardiofacial syndrome (VCFS), also known as DiGeorge, conotruncal anomaly face, and Cayler syndr...
Item does not contain fulltextThe velo-cardio-facial syndrome (VCFS) is a leading cause of velophary...
BACKGROUND: As children with velocardiofacial syndrome (VCFS) develop, they are at increased risk fo...
In this contribution the current status and recent findings of the behavioural phenotype in VCFS (22...
Among the many features with which velocardiofacial syndrome (VCFS) may present, we review in this p...
Velocardiofacial syndrome, also called Shprintzen syndrome or DiGeorge sequence, is one of the most ...
Background Velocardiofacial syndrome (VCFS) is a microdeletion syndrome caused by a 22q11.2 chromoso...
In this contribution the current status and recent findings of the behavioural phenotype in VCFS (22...
Objective—Velo-cardio-facial syndrome (VCFS) is caused by a microdeletion of approximately 40 genes ...
Purpose of review: The understanding of velo-cardio-facial syndrome has grown markedly since the ini...
The extent to which the phenotype of children comorbid for velocardiofacial syndrome (VCFS) and auti...