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A O Edwards

Showing results (1-10 of 10) with videos related to

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Eye (London, England)|March 1, 2008
Clinical features of the congenital vitreoretinopathiesA O Edwards
Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.)|April 1, 1987
Effects of hypophysectomy on plasma levels of pancreatic polypeptide (APP) and insulin in adult chickensA O Edwards, R L Hazelwood
Investigative Ophthalmology & Visual Science|October 3, 2001
A novel gene for autosomal dominant Stargardt-like macular dystrophy with homology to the SUR4 protein familyA O Edwards, L A Donoso, R Ritter
American Journal of Ophthalmology|December 4, 2001
Renal-coloboma syndrome: report of a novel PAX2 gene mutationG W Chung, A O Edwards, L A Schimmenti, et al.
Survey of Ophthalmology|October 2, 2001
Autosomal dominant Stargardt-like macular dystrophyL A Donoso, A O Edwards, A Frost, et al.
American Journal of Ophthalmology|April 28, 1999
Autosomal dominant Stargardt-like macular dystrophy: I. Clinical characterization, longitudinal follow-up, and evidence for a common ancestry in families linked to chromosome 6q14A O Edwards, A Miedziak, T Vrabec, 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.
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.
Archives of Ophthalmology (Chicago, Ill. : 1960)|April 25, 2001
Autosomal dominant Stargardt-like macular dystrophy: founder effect and reassessment of genetic heterogeneityL A Donoso, A T Frost, E M Stone, et al.
Human Molecular Genetics|April 3, 2010
Transcriptome analysis and molecular signature of human retinal pigment epitheliumN V Strunnikova, A Maminishkis, J J Barb, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Eye (London, England)|March 1, 2008
Clinical features of the congenital vitreoretinopathiesA O Edwards
Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.)|April 1, 1987
Effects of hypophysectomy on plasma levels of pancreatic polypeptide (APP) and insulin in adult chickensA O Edwards, R L Hazelwood
Investigative Ophthalmology & Visual Science|October 3, 2001
A novel gene for autosomal dominant Stargardt-like macular dystrophy with homology to the SUR4 protein familyA O Edwards, L A Donoso, R Ritter
American Journal of Ophthalmology|December 4, 2001
Renal-coloboma syndrome: report of a novel PAX2 gene mutationG W Chung, A O Edwards, L A Schimmenti, et al.
Survey of Ophthalmology|October 2, 2001
Autosomal dominant Stargardt-like macular dystrophyL A Donoso, A O Edwards, A Frost, et al.
American Journal of Ophthalmology|April 28, 1999
Autosomal dominant Stargardt-like macular dystrophy: I. Clinical characterization, longitudinal follow-up, and evidence for a common ancestry in families linked to chromosome 6q14A O Edwards, A Miedziak, T Vrabec, 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.
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.
Archives of Ophthalmology (Chicago, Ill. : 1960)|April 25, 2001
Autosomal dominant Stargardt-like macular dystrophy: founder effect and reassessment of genetic heterogeneityL A Donoso, A T Frost, E M Stone, et al.
Human Molecular Genetics|April 3, 2010
Transcriptome analysis and molecular signature of human retinal pigment epitheliumN V Strunnikova, A Maminishkis, J J Barb, et al.
Pageof 1