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American Journal of Human Genetics|April 1, 1994
Further refinement of the location for autosomal dominant retinitis pigmentosa on chromosome 7p (RP9)C F Inglehearn, T J Keen, M al-Maghtheh, et al.The British Journal of Ophthalmology|August 1, 1992
Abnormal dark adaptation kinetics in autosomal dominant sector retinitis pigmentosa due to rod opsin mutationA T Moore, F W Fitzke, C M Kemp, et al.Journal of Medical Genetics|November 1, 1994
Retinitis pigmentosa families showing apparent X linked inheritance but unlinked to the RP2 or RP3 lociM A Aldred, P W Teague, M Jay, et al.Human Genetics|March 10, 1999
Refined genetic and physical positioning of the gene for Doyne honeycomb retinal dystrophy (DHRD)S Kermani, K Gregory-Evans, E E Tarttelin, et al.Journal of Immunological Methods|June 26, 1987
An improved method for the purification of retinal S-antigen using selective hydrophobic adsorption chromatographyE Kasp, J P Banga, E C Brown, et al.The British Journal of Ophthalmology|January 30, 1999
Phenotype of a British North Carolina macular dystrophy family linked to chromosome 6qM B Reichel, R E Kelsell, J Fan, et al.The British Journal of Ophthalmology|May 23, 2006
Clinical characterisation of a family with retinal dystrophy caused by mutation in the Mertk geneM Tschernutter, S A Jenkins, N H Waseem, et al.Journal of Medical Genetics|July 1, 1991
Genetic localisation of the RP2 type of X linked retinitis pigmentosa in a large kindredA F Wright, S S Bhattacharya, M A Aldred, et al.Human Molecular Genetics|September 1, 1995
Localization of the gene for progressive bifocal chorioretinal atrophy (PBCRA) to chromosome 6qR E Kelsell, B F Godley, K Evans, et al.American Journal of Human Genetics|March 1, 1992
Recombination between rhodopsin and locus D3S47 (C17) in rhodopsin retinitis pigmentosa familiesC F Inglehearn, D H Lester, R Bashir, et al.Pageof 33