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G A Fishman

Showing results (181-190 of 224) with videos related to

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American Journal of Human Genetics|October 1, 1991
Identification of novel rhodopsin mutations associated with retinitis pigmentosa by GC-clamped denaturing gradient gel electrophoresisV C Sheffield, G A Fishman, J S Beck, et al.
Experimental Eye Research|September 1, 1996
Sinclair swine with spontaneously regressing cutaneous melanomas do not have autoantibodies against retinal bipolar cellsK R Alexander, G A Fishman, R W Swinfard, et al.
Applied Optics|June 16, 2010
Rod increment thresholds in cone-rod dystrophyD W Yates, D J Derlacki, D R Pepperberg, et al.
Ophthalmic Paediatrics and Genetics|August 1, 1984
Retrospective analysis of 58 children with retinoblastomaL Mathew, T D Miale, S Rao, et al.
Ophthalmology|January 11, 2001
Perceived and actual performance of daily tasks: relationship to visual function tests in individuals with retinitis pigmentosaJ P Szlyk, W Seiple, G A Fishman, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|February 1, 1982
Autosomal dominant vitreoretinochoroidopathyS J Kaufman, M F Goldberg, D H Orth, et al.
Ophthalmology|November 1, 1993
Visual acuity in patients with best vitelliform macular dystrophyG A Fishman, W Baca, K R Alexander, et al.
Human Molecular Genetics|November 1, 1993
Polymorphisms and rare sequence variants at the ROM1 locusR A Bascom, L Liu, P Humphries, et al.
Ophthalmology|August 1, 1994
Clinical features of a previously undescribed codon 216 (proline to serine) mutation in the peripherin/retinal degeneration slow gene in autosomal dominant retinitis pigmentosaG A Fishman, E Stone, L D Gilbert, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 18, 1998
Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or leber congenital amaurosisH Morimura, G A Fishman, S A Grover, et al.
Pageof 23

Showing results (181-190 of 224) with videos related to

Sort By:
Pageof 23
American Journal of Human Genetics|October 1, 1991
Identification of novel rhodopsin mutations associated with retinitis pigmentosa by GC-clamped denaturing gradient gel electrophoresisV C Sheffield, G A Fishman, J S Beck, et al.
Experimental Eye Research|September 1, 1996
Sinclair swine with spontaneously regressing cutaneous melanomas do not have autoantibodies against retinal bipolar cellsK R Alexander, G A Fishman, R W Swinfard, et al.
Applied Optics|June 16, 2010
Rod increment thresholds in cone-rod dystrophyD W Yates, D J Derlacki, D R Pepperberg, et al.
Ophthalmic Paediatrics and Genetics|August 1, 1984
Retrospective analysis of 58 children with retinoblastomaL Mathew, T D Miale, S Rao, et al.
Ophthalmology|January 11, 2001
Perceived and actual performance of daily tasks: relationship to visual function tests in individuals with retinitis pigmentosaJ P Szlyk, W Seiple, G A Fishman, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|February 1, 1982
Autosomal dominant vitreoretinochoroidopathyS J Kaufman, M F Goldberg, D H Orth, et al.
Ophthalmology|November 1, 1993
Visual acuity in patients with best vitelliform macular dystrophyG A Fishman, W Baca, K R Alexander, et al.
Human Molecular Genetics|November 1, 1993
Polymorphisms and rare sequence variants at the ROM1 locusR A Bascom, L Liu, P Humphries, et al.
Ophthalmology|August 1, 1994
Clinical features of a previously undescribed codon 216 (proline to serine) mutation in the peripherin/retinal degeneration slow gene in autosomal dominant retinitis pigmentosaG A Fishman, E Stone, L D Gilbert, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 18, 1998
Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or leber congenital amaurosisH Morimura, G A Fishman, S A Grover, et al.
Pageof 23