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Ophthalmic Genetics - ResearchHub

Journal

Ophthalmic Genetics

1381-6810 · Informa UK Limited

8 verified public works

Browse all journals →

Late onset retinoblastoma in a child with 13 q deletion syndrome

2026 · 0 citations

Retinitis Pigmentosa and erythrocytic microcytosis related to hypomorphic variants in the TRNT1 gene

2026 · 0 citations

Patient- and caregiver-reported outcomes in Bardet-Biedl syndrome: a scoping review

2026 · 0 citations

Anterior segment dysgenesis with bilateral acorea and microphthalmia associated with compound heterozygous FOXE3 pathogenic variants: outcomes after optical iridectomy

2026 · 0 citations

Norrie disease with asymmetric retinal severity associated with novel NDP variants

2026 · 0 citations

Beyond corneal structure in Noonan syndrome: topographic, tomographic, and optical findings

2026 · 0 citations

Isolated rod-cone dystrophy in homozygous IFT140 missense allele p.Tyr923Asp

2026 · 0 citations

Genetic findings and clinical features of extreme refractive errors in Thai children using whole genome sequencing

2026 · 0 citations

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