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Survey of Ophthalmology|March 1, 1995
An international classification and grading system for age-related maculopathy and age-related macular degeneration. The International ARM Epidemiological Study GroupA C Bird, N M Bressler, S B Bressler, et al.
The British Journal of Ophthalmology|July 19, 2005
Visual functioning and quality of life in the SubFoveal Radiotherapy Study (SFRADS): SFRADS report 2M R Stevenson, P M Hart, U Chakravarthy, et al.
Nature|May 17, 1984
Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28S S Bhattacharya, A F Wright, J F Clayton, et al.
Experimental Eye Research|April 20, 2001
Spectrum of mutations in USH2A in British patients with Usher syndrome type IIB P Leroy, J A Aragon-Martin, M D Weston, et al.
Investigative Ophthalmology & Visual Science|November 30, 2000
RP1 protein truncating mutations predominate at the RP1 adRP locusA Payne, E Vithana, S Khaliq, et al.
Molecular Cell|September 8, 2001
A human homolog of yeast pre-mRNA splicing gene, PRP31, underlies autosomal dominant retinitis pigmentosa on chromosome 19q13.4 (RP11)E N Vithana, L Abu-Safieh, M J Allen, et al.
Ophthalmology|January 27, 2000
Autosomal dominant cone-rod retinal dystrophy (CORD6) from heterozygous mutation of GUCY2D, which encodes retinal guanylate cyclaseK Gregory-Evans, R E Kelsell, C Y Gregory-Evans, et al.
Nature Genetics|June 16, 1999
A single EFEMP1 mutation associated with both Malattia Leventinese and Doyne honeycomb retinal dystrophyE M Stone, A J Lotery, F L Munier, et al.
Human Molecular Genetics|July 27, 2001
Mutations in the pre-mRNA splicing factor gene PRPC8 in autosomal dominant retinitis pigmentosa (RP13)A B McKie, J C McHale, T J Keen, et al.
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