Found: 3
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Familial aniridia spectrum in four families of Czech origin with PAX6 mutations.
- Published in:
- Acta Ophthalmologica (1755375X), 2019, v. 97, p. N.PAG, doi. 10.1111/j.1755-3768.2019.5365
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- Publication type:
- Article
Leber congenital amaurosis and early onset severe retinal dystrophy in the Czech Republic: Mutational spectrum and clinical findings.
- Published in:
- 2022
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- Publication type:
- Abstract
Comprehensive phenotypic and functional analysis of dominant and recessive FOXE3 alleles in ocular developmental disorders.
- Published in:
- Human Molecular Genetics, 2021, v. 30, n. 17, p. 1591, doi. 10.1093/hmg/ddab142
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- Publication type:
- Article