Identification of a novel de novo variant in OTX2 in a patient with congenital microphthalmia using targeted next-generation sequencing followed by prenatal diagnosis.
Ophthalmic Genet
; 43(2): 262-267, 2022 04.
Article
in En
| MEDLINE
| ID: mdl-34791963
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Microphthalmos
Type of study:
Diagnostic_studies
/
Prognostic_studies
Limits:
Female
/
Humans
/
Pregnancy
Language:
En
Journal:
Ophthalmic Genet
Journal subject:
GENETICA MEDICA
/
OFTALMOLOGIA
Year:
2022
Document type:
Article
Affiliation country:
Country of publication: