Clinical and molecular characterization of an emerging chromosome 22q13.31 microdeletion syndrome.
Am J Med Genet A
; 176(2): 391-398, 2018 02.
Article
in En
| MEDLINE
| ID: mdl-29193617
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Developmental Disabilities
/
Chromosome Disorders
/
Neurodevelopmental Disorders
Type of study:
Prognostic_studies
Limits:
Adolescent
/
Humans
/
Male
Language:
En
Journal:
Am J Med Genet A
Journal subject:
GENETICA MEDICA
Year:
2018
Type:
Article
Affiliation country:
Italy