# Ophthalmic Genetics

**Type:** Journals  
**Canonical URL:** https://scholariq.org/journals/ophthalmic-genetics/

## Facts

| Field | Value |
| --- | --- |
| Open Access | false |
| ISSN-L | 1381-6810 |
| ISSNs | 1381-6810,1744-5094 |
| OpenAlex ID | https://openalex.org/S12713009 |
| Publisher | Taylor & Francis |

## Journal papers

- [Ocular findings in 55 patients with Down's syndrome](https://scholariq.org/papers/ocular-findings-in-55-patients-with-down-s-syndrome/)
- [The clinical evaluation of infantile nystagmus: What to do first and why](https://scholariq.org/papers/the-clinical-evaluation-of-infantile-nystagmus-what-to-do-first-and-why/)
- [Retinal disease in the C3 glomerulopathies and the risk of impaired vision](https://scholariq.org/papers/retinal-disease-in-the-c3-glomerulopathies-and-the-risk-of-impaired-vision/)
- [Living with Stargardt disease: insights from patients and their parents](https://scholariq.org/papers/living-with-stargardt-disease-insights-from-patients-and-their-parents/)
- [Further delineation of the oculoauricular syndrome phenotype: A new family with a novel truncating HMX1 mutation](https://scholariq.org/papers/further-delineation-of-the-oculoauricular-syndrome-phenotype-a-new-family-with-a/)
- [A novel <i>LTBP2</i> gene variant in a Turkish family with juvenile-onset open-angle glaucoma](https://scholariq.org/papers/a-novel-i-ltbp2-i-gene-variant-in-a-turkish-family-with-juvenile-onset-open/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.
