A novel de novo 1.8 Mb microdeletion of 17q21.33 associated with intellectual disability and dysmorphic features.
Eur J Med Genet
; 55(11): 656-9, 2012 Nov.
Article
in En
| MEDLINE
| ID: mdl-22842074
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Abnormalities, Multiple
/
Muscular Atrophy
/
Intellectual Disability
Type of study:
Diagnostic_studies
/
Risk_factors_studies
Limits:
Adolescent
/
Humans
/
Male
Language:
En
Journal:
Eur J Med Genet
Year:
2012
Document type:
Article