Genetic etiology study of four Chinese families with two nonsyndromic deaf children in succession by targeted next-generation sequencing.
Mol Genet Genomic Med
; 9(4): e1634, 2021 04.
Article
in En
| MEDLINE
| ID: mdl-33638616
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Genetic Heterogeneity
/
Hearing Loss, Sensorineural
Type of study:
Etiology_studies
Limits:
Adolescent
/
Adult
/
Child
/
Child, preschool
/
Female
/
Humans
/
Male
/
Middle aged
/
Newborn
Language:
En
Journal:
Mol Genet Genomic Med
Year:
2021
Document type:
Article
Affiliation country:
China
Country of publication:
United States