De novo variants in CDK13 associated with syndromic ID/DD: Molecular and clinical delineation of 15 individuals and a further review.
Clin Genet
; 93(5): 1000-1007, 2018 05.
Article
in En
| MEDLINE
| ID: mdl-29393965
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Developmental Disabilities
/
CDC2 Protein Kinase
/
Heart Defects, Congenital
/
Intellectual Disability
Type of study:
Prognostic_studies
/
Risk_factors_studies
Limits:
Adolescent
/
Adult
/
Child
/
Child, preschool
/
Female
/
Humans
/
Male
/
Middle aged
Language:
En
Journal:
Clin Genet
Year:
2018
Document type:
Article
Affiliation country:
Países Bajos
Country of publication:
Dinamarca