Identification of a novel mutation in the FGF10 gene in a Chinese family with obvious congenital lacrimal duct dysplasia in lacrimo-auriculo-dento-digital syndrome.
Int J Ophthalmol
; 16(4): 499-504, 2023.
Article
in En
| MEDLINE
| ID: mdl-37077496
Full text:
1
Database:
MEDLINE
Type of study:
Diagnostic_studies
/
Guideline
/
Prognostic_studies
Language:
En
Year:
2023
Type:
Article