Review of neurodevelopmental disorders in patients with HNF1B gene variations.
Front Pediatr
; 11: 1149875, 2023.
Article
in En
| MEDLINE
| ID: mdl-36969268
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Type of study:
Prognostic_studies
/
Risk_factors_studies
Language:
En
Journal:
Front Pediatr
Year:
2023
Document type:
Article
Affiliation country:
Germany
Country of publication:
Switzerland