Clinical and molecular characterization of the 20q11.2 microdeletion syndrome: six new patients.
Am J Med Genet A
; 167A(3): 504-11, 2015 Mar.
Article
in En
| MEDLINE
| ID: mdl-25572454
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Phenotype
/
Abnormalities, Multiple
/
Chromosomes, Human, Pair 20
/
Chromosome Deletion
Type of study:
Prognostic_studies
Limits:
Adolescent
/
Adult
/
Child
/
Child, preschool
/
Female
/
Humans
/
Infant
/
Male
Language:
En
Journal:
Am J Med Genet A
Journal subject:
GENETICA MEDICA
Year:
2015
Document type:
Article
Affiliation country:
Francia