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Last Updated : 06/20/2022

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Found 19 publications

Burden of ocular morbidities and color blindness among school-attending children in a foothill town of Uttarakhand State.

Implications of inherited color vision deficiency on occupations: A neglected entity!

Clinically relevant colour album test for the colour defective medical student.

Oscillatory Potentials in Achromatopsia as a Tool for Understanding Cone Retinal Functions.

Acute bilateral retrobulbar optic neuritis - An atypical sequela of COVID-19.

Identification of a novel RPGR mutation associated with X-linked cone-rod dystrophy in a Chinese family.

A deep intronic substitution in CNGB3 is one of the major causes of achromatopsia among Jewish patients.

The Effects of a Blue-Light Filtering Versus Clear Intraocular Implant on Color Appearance.

Blue Cone Monochromatism with Foveal Hypoplasia Caused by the Concomitant Effect of Variants in OPN1LW/OPN1MW and GPR143 Genes.

Paternal Uniparental Isodisomy of Chromosome 2 in a Patient with CNGA3-Associated Autosomal Recessive Achromatopsia.

Non-syndromic inherited retinal diseases in Poland: Genes, mutations, and phenotypes.

Prevalence of color vision deficiency among school-going boys in South India.

Showing 1-12 of 19

Last Updated : 06/20/2022