In this contribution the current status and recent findings of the behavioural phenotype in VCFS (22q11 deletion) are discussed with regard to motor development, cognition and neurodevelopment, and behaviour and temperament. Motor: hypotonia in infancy gross-motor milestones are delayed, problems with coordination and balance from preschool age on, problems with tempo/speed during adolescence. Cognition and neurodevelopment: learning disabilities (82-100%), intellectual disability (45%), better verbal abilities than performal abilities, poor attention and concentration, visuo-perceptual-spatial problems, good (auditory) memory. An important subgroup of children (55%) has a non-verbal learning disability (NLD). Behaviour and social-emotional...
Velo-cardio-facial syndrome (VCFS) is a genetic disorder caused by a microdeletion of chromosome 22q...
Parenting, family contexts, and personality characteristics in youngsters with VCFS: The personality...
Velo-cardio-facial syndrome (VCFS) is associated with deletions on the long arm of chromosome 22, mi...
In this contribution the current status and recent findings of the behavioural phenotype in VCFS (22...
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...
The velo-cardio-facial syndrome: the spectrum of psychiatric problems and cognitive deterioration at...
The personality profile of 48 youngsters (24 males and 24 females, mean age 8 years, 5 months) with ...
The personality profile of 48 youngsters (24 males and 24 females, mean age 8 years, 5 months) with ...
Velocardiofacial syndrome (VCFS) is one of the most common genetic disorders that affect every major...
Velo-cardio-facial syndrome (vcfs) is a congenital disorder with a markedly variable clinical expres...
Background Velocardiofacial syndrome (VCFS) is a microdeletion syndrome caused by a 22q11.2 chromoso...
Background Learning disabilities are one of the most consistently reported features in Velo–Cardio– ...
Children with a 22q11 deletion versus children with a speech-language impairment and learning disabi...
of the present study was to examine the previously reported mathematical disabilities (MD) of childr...
Velo-cardio-facial syndrome (VCFS) is a genetic disorder caused by a microdeletion of chromosome 22q...
Parenting, family contexts, and personality characteristics in youngsters with VCFS: The personality...
Velo-cardio-facial syndrome (VCFS) is associated with deletions on the long arm of chromosome 22, mi...
In this contribution the current status and recent findings of the behavioural phenotype in VCFS (22...
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...
The velo-cardio-facial syndrome: the spectrum of psychiatric problems and cognitive deterioration at...
The personality profile of 48 youngsters (24 males and 24 females, mean age 8 years, 5 months) with ...
The personality profile of 48 youngsters (24 males and 24 females, mean age 8 years, 5 months) with ...
Velocardiofacial syndrome (VCFS) is one of the most common genetic disorders that affect every major...
Velo-cardio-facial syndrome (vcfs) is a congenital disorder with a markedly variable clinical expres...
Background Velocardiofacial syndrome (VCFS) is a microdeletion syndrome caused by a 22q11.2 chromoso...
Background Learning disabilities are one of the most consistently reported features in Velo–Cardio– ...
Children with a 22q11 deletion versus children with a speech-language impairment and learning disabi...
of the present study was to examine the previously reported mathematical disabilities (MD) of childr...
Velo-cardio-facial syndrome (VCFS) is a genetic disorder caused by a microdeletion of chromosome 22q...
Parenting, family contexts, and personality characteristics in youngsters with VCFS: The personality...
Velo-cardio-facial syndrome (VCFS) is associated with deletions on the long arm of chromosome 22, mi...