Further delineation of the KBG syndrome phenotype caused by ANKRD11 aberrations.
Eur J Hum Genet
; 23(9): 1176-85, 2015 Sep.
Article
in En
| MEDLINE
| ID: mdl-25424714
Full text:
1
Database:
MEDLINE
Main subject:
Repressor Proteins
/
Tooth Abnormalities
/
Abnormalities, Multiple
/
Bone Diseases, Developmental
/
Chromosomes, Human, Pair 16
/
Gene Deletion
/
Autism Spectrum Disorder
/
Intellectual Disability
Type of study:
Diagnostic_studies
/
Prognostic_studies
Limits:
Adolescent
/
Adult
/
Child
/
Child, preschool
/
Female
/
Humans
/
Male
/
Middle aged
Language:
En
Journal:
Eur J Hum Genet
Journal subject:
GENETICA MEDICA
Year:
2015
Type:
Article
Affiliation country:
Netherlands