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The British Journal of Ophthalmology|July 22, 1999
Phenotype of autosomal recessive congenital microphthalmia mapping to chromosome 14q32D A Bessant, K Anwar, S Khaliq, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|April 1, 1995
Autosomal dominant pattern dystrophy of the retina associated with a 4-base pair insertion at codon 140 in the peripherin/RDS geneR Y Kim, H Dollfus, T J Keen, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|November 1, 1993
Dominant retinitis pigmentosa associated with two rhodopsin gene mutations. Leu-40-Arg and an insertion disrupting the 5'-splice junction of exon 5R Y Kim, M al-Maghtheh, F W Fitzke, et al.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.Archives of Ophthalmology (Chicago, Ill. : 1960)|September 1, 1985
Accuracy of detection of the retinoblastoma gene by esterase D linkageS L Halloran, J A Boughman, T P Dryja, 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.Pageof 37