The CHD4-related syndrome: a comprehensive investigation of the clinical spectrum, genotype-phenotype correlations, and molecular basis.
Genet Med
; 22(2): 389-397, 2020 02.
Article
in En
| MEDLINE
| ID: mdl-31388190
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Mi-2 Nucleosome Remodeling and Deacetylase Complex
/
Neurodevelopmental Disorders
Type of study:
Prognostic_studies
Limits:
Adolescent
/
Adult
/
Child
/
Child, preschool
/
Female
/
Humans
/
Infant
/
Male
/
Newborn
Language:
En
Journal:
Genet Med
Year:
2020
Document type:
Article