Rare copy number variation analysis identifies disease-related variants in atrioventricular septal defect patients.
Front Genet
; 14: 1075349, 2023.
Article
in En
| MEDLINE
| ID: mdl-36816019
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Type of study:
Prognostic_studies
Language:
En
Journal:
Front Genet
Year:
2023
Document type:
Article
Affiliation country:
China
Country of publication:
Suiza