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Investigative Ophthalmology & Visual Science|October 29, 2000
Novel locus for autosomal recessive cone-rod dystrophy CORD8 mapping to chromosome 1q12-Q24S Khaliq, A Hameed, M Ismail, et al.Human Molecular Genetics|August 1, 1995
An eighth locus for autosomal dominant retinitis pigmentosa is linked to chromosome 17qS Bardien, N Ebenezer, J Greenberg, et al.Human Mutation|September 12, 2000
Sequence variation within the RPGR gene: evidence for a founder complex alleleI Zito, A Morris, P Tyson, et al.Human Mutation|June 22, 2000
Novel frameshift mutations in the RP2 gene and polymorphic variantsD L Thiselton, I Zito, C Plant, et al.Eye (London, England)|January 1, 1995
The role of molecular genetics in the prenatal diagnosis of retinal dystrophiesK Evans, C Y Gregory, A Fryer, et al.The British Journal of Ophthalmology|May 1, 1985
A genetic linkage study of a kindred with X-linked retinitis pigmentosaS S Bhattacharya, J F Clayton, P S Harper, et al.Genomics|September 1, 1991
Autosomal dominant retinitis pigmentosa: four new mutations in rhodopsin, one of them in the retinal attachment siteT J Keen, C F Inglehearn, D H Lester, et al.Annals of Human Genetics|September 7, 2007
Genetic analysis of FAM46A in Spanish families with autosomal recessive retinitis pigmentosa: characterisation of novel VNTRsI Barragán, S Borrego, M M Abd El-Aziz, et al.Human Molecular Genetics|September 26, 2000
Functional impairment of lens aquaporin in two families with dominantly inherited cataractsP Francis, J J Chung, M Yasui, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|October 26, 1999
Clinical features of codon 172 RDS macular dystrophy: similar phenotype in 12 familiesS M Downes, F W Fitzke, G E Holder, et al.Pageof 18