Comprehensive genomic diagnosis of non-syndromic and syndromic hereditary hearing loss in Spanish patients.
BMC Med Genomics
; 11(1): 58, 2018 Jul 09.
Article
in En
| MEDLINE
| ID: mdl-29986705
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Genomics
/
Hearing Loss
Type of study:
Diagnostic_studies
/
Prognostic_studies
Limits:
Adolescent
/
Adult
/
Child
/
Child, preschool
/
Female
/
Humans
/
Infant
/
Male
/
Middle aged
/
Newborn
Country/Region as subject:
Europa
Language:
En
Journal:
BMC Med Genomics
Journal subject:
GENETICA MEDICA
Year:
2018
Document type:
Article
Affiliation country:
España
Country of publication:
Reino Unido