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B Arden

Showing results (171-180 of 178) with videos related to

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The British Journal of Ophthalmology|January 1, 1995
Autosomal dominant retinitis pigmentosa mapping to chromosome 7p exhibits variable expressionR Y Kim, F W Fitzke, A T Moore, et al.
The British Journal of Ophthalmology|May 1, 1985
A clinical, psychophysical, and electroretinographic survey of patients with autosomal dominant retinitis pigmentosaA L Lyness, W Ernst, M P Quinlan, et al.
The British Journal of Ophthalmology|May 1, 1994
Ocular manifestations in autosomal dominant retinitis pigmentosa with a Lys-296-Glu rhodopsin mutation at the retinal binding siteS L Owens, F W Fitzke, C F Inglehearn, et al.
Ophthalmology|January 1, 1994
Macular dystrophy associated with mutations at codon 172 in the human retinal degeneration slow geneJ J Wroblewski, J A Wells, A Eckstein, et al.
The British Journal of Ophthalmology|July 1, 1983
Rod and cone activity in patients with dominantly inherited retinitis pigmentosa: comparisons between psychophysical and electroretinographic measurementsG B Arden, R M Carter, C R Hogg, et al.
The British Journal of Ophthalmology|July 1, 1983
A modified ERG technique and the results obtained in X-linked retinitis pigmentosaG B Arden, R M Carter, C R Hogg, 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.
The British Journal of Ophthalmology|November 1, 1994
Ocular findings associated with a 3 base pair deletion in the peripherin-RDS gene in autosomal dominant retinitis pigmentosaJ J Wroblewski, J A Wells, A Eckstein, et al.
Pageof 18

Showing results (171-180 of 178) with videos related to

Sort By:
Pageof 18
You have reached the last page of results.This site can display upto 178 results.
The British Journal of Ophthalmology|January 1, 1995
Autosomal dominant retinitis pigmentosa mapping to chromosome 7p exhibits variable expressionR Y Kim, F W Fitzke, A T Moore, et al.
The British Journal of Ophthalmology|May 1, 1985
A clinical, psychophysical, and electroretinographic survey of patients with autosomal dominant retinitis pigmentosaA L Lyness, W Ernst, M P Quinlan, et al.
The British Journal of Ophthalmology|May 1, 1994
Ocular manifestations in autosomal dominant retinitis pigmentosa with a Lys-296-Glu rhodopsin mutation at the retinal binding siteS L Owens, F W Fitzke, C F Inglehearn, et al.
Ophthalmology|January 1, 1994
Macular dystrophy associated with mutations at codon 172 in the human retinal degeneration slow geneJ J Wroblewski, J A Wells, A Eckstein, et al.
The British Journal of Ophthalmology|July 1, 1983
Rod and cone activity in patients with dominantly inherited retinitis pigmentosa: comparisons between psychophysical and electroretinographic measurementsG B Arden, R M Carter, C R Hogg, et al.
The British Journal of Ophthalmology|July 1, 1983
A modified ERG technique and the results obtained in X-linked retinitis pigmentosaG B Arden, R M Carter, C R Hogg, 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.
The British Journal of Ophthalmology|November 1, 1994
Ocular findings associated with a 3 base pair deletion in the peripherin-RDS gene in autosomal dominant retinitis pigmentosaJ J Wroblewski, J A Wells, A Eckstein, et al.
Pageof 18