Correction: Exome sequencing in infants with congenital hearing impairment: a population-based cohort study.
Eur J Hum Genet
; 29(2): 363, 2021 Feb.
Article
in En
| MEDLINE
| ID: mdl-33168987
Full text:
1
Database:
MEDLINE
Type of study:
Etiology_studies
/
Observational_studies
Language:
En
Journal:
Eur J Hum Genet
Journal subject:
GENETICA MEDICA
Year:
2021
Type:
Article
Affiliation country:
Australia