Related Experiment Videos

[Hydrophilic contact lenses]

Nederlands Tijdschrift Voor Geneeskunde

|June 15, 1974

Summary

No abstract available in PubMed .

Related Concept Videos

Articles linked to this work by shared authors, journal, and citation graph.

Null mutation in the human 11-cis retinol dehydrogenase gene associated with fundus albipunctatus.

Ophthalmology·2001

Predictive value of pattern VEP, pattern ERG and hole size in macular hole surgery.

Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie·1999

Phenotypic variations in a family with retinal dystrophy as result of different mutations in the ABCR gene.

The British journal of ophthalmology·1999

The 2588G-->C mutation in the ABCR gene is a mild frequent founder mutation in the Western European population and allows the classification of ABCR mutations in patients with Stargardt disease.

American journal of human genetics·1999

Refined mapping of the gene for autosomal dominant retinitis pigmentosa (RP17) on chromosome 17q22.

Human genetics·1999

Positional cloning of the gene for X-linked retinitis pigmentosa 2.

Nature genetics·1998

See all related articles