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R G Weleber

Showing results (71-80 of 110) with videos related to

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Human Molecular Genetics|August 13, 1998
Localization of dystrophin isoform Dp71 to the inner limiting membrane of the retina suggests a unique functional contribution of Dp71 in the retinaP L Howard, G Y Dally, M H Wong, et al.
The British Journal of Ophthalmology|May 30, 2002
Retrospective, longitudinal, and cross sectional study of visual acuity impairment in choroideraemiaM Flynn Roberts, G A Fishman, D K Roberts, et al.
Investigative Ophthalmology & Visual Science|July 1, 1988
Expression defect of ornithine aminotransferase gene in gyrate atrophyG Inana, Y Hotta, C Zintz, et al.
American Journal of Human Genetics|April 1, 1990
Cosegregation of elastin-associated microfibrillar abnormalities with the Marfan phenotype in familiesM Godfrey, V Menashe, R G Weleber, et al.
Journal of Medical Genetics|June 5, 2001
Molecular genetic heterogeneity in autosomal dominant drusenE E Tarttelin, C Y Gregory-Evans, A C Bird, et al.
Brain Research|June 28, 1988
Dose-response relationship between light irradiance and the suppression of plasma melatonin in human volunteersG C Brainard, A J Lewy, M Menaker, et al.
Investigative Ophthalmology & Visual Science|September 28, 2000
HRG4 (UNC119) mutation found in cone-rod dystrophy causes retinal degeneration in a transgenic modelA Kobayashi, T Higashide, D Hamasaki, et al.
Ophthalmology|September 15, 1999
Visual acuity impairment in patients with retinitis pigmentosa at age 45 years or olderS Grover, G A Fishman, R J Anderson, et al.
Genomics|May 20, 1995
A heterozygous putative null mutation in ROM1 without a mutation in peripherin/RDS in a family with retinitis pigmentosaH Sakuma, G Inana, A Murakami, et al.
American Journal of Ophthalmology|September 23, 1998
Malattia leventinese: refinement of the genetic locus and phenotypic variability in autosomal dominant macular drusenA O Edwards, M L Klein, C B Berselli, et al.
Pageof 11

Showing results (71-80 of 110) with videos related to

Sort By:
Pageof 11
Human Molecular Genetics|August 13, 1998
Localization of dystrophin isoform Dp71 to the inner limiting membrane of the retina suggests a unique functional contribution of Dp71 in the retinaP L Howard, G Y Dally, M H Wong, et al.
The British Journal of Ophthalmology|May 30, 2002
Retrospective, longitudinal, and cross sectional study of visual acuity impairment in choroideraemiaM Flynn Roberts, G A Fishman, D K Roberts, et al.
Investigative Ophthalmology & Visual Science|July 1, 1988
Expression defect of ornithine aminotransferase gene in gyrate atrophyG Inana, Y Hotta, C Zintz, et al.
American Journal of Human Genetics|April 1, 1990
Cosegregation of elastin-associated microfibrillar abnormalities with the Marfan phenotype in familiesM Godfrey, V Menashe, R G Weleber, et al.
Journal of Medical Genetics|June 5, 2001
Molecular genetic heterogeneity in autosomal dominant drusenE E Tarttelin, C Y Gregory-Evans, A C Bird, et al.
Brain Research|June 28, 1988
Dose-response relationship between light irradiance and the suppression of plasma melatonin in human volunteersG C Brainard, A J Lewy, M Menaker, et al.
Investigative Ophthalmology & Visual Science|September 28, 2000
HRG4 (UNC119) mutation found in cone-rod dystrophy causes retinal degeneration in a transgenic modelA Kobayashi, T Higashide, D Hamasaki, et al.
Ophthalmology|September 15, 1999
Visual acuity impairment in patients with retinitis pigmentosa at age 45 years or olderS Grover, G A Fishman, R J Anderson, et al.
Genomics|May 20, 1995
A heterozygous putative null mutation in ROM1 without a mutation in peripherin/RDS in a family with retinitis pigmentosaH Sakuma, G Inana, A Murakami, et al.
American Journal of Ophthalmology|September 23, 1998
Malattia leventinese: refinement of the genetic locus and phenotypic variability in autosomal dominant macular drusenA O Edwards, M L Klein, C B Berselli, et al.
Pageof 11