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E M Stone

Showing results (101-110 of 174) with videos related to

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Ophthalmic Genetics|November 12, 1998
Rhodopsin C110Y mutation causes a type 2 autosomal dominant retinitis pigmentosaE Millá, E Héon, P A Grounauer, et al.
Nature Genetics|December 8, 1998
Allelic variation in ABCR associated with Stargardt disease but not age-related macular degenerationE M Stone, A R Webster, K Vandenburgh, et al.
Investigative Ophthalmology & Visual Science|August 1, 1996
Sub-retinal pigment epithelial deposits in a dominant late-onset retinal degenerationC A Kuntz, S G Jacobson, A V Cideciyan, et al.
Ophthalmology|October 1, 1992
Avellino corneal dystrophy. Clinical manifestations and natural historyE J Holland, S M Daya, E M Stone, et al.
American Journal of Ophthalmology|January 23, 1998
Autosomal dominant iris hypoplasia is caused by a mutation in the Rieger syndrome (RIEG/PITX2) geneW L Alward, E V Semina, J W Kalenak, et al.
Genome Research|September 1, 1996
Fine mapping of the autosomal dominant juvenile open angle glaucoma (GLC1A) region and evaluation of candidate genesS L Sunden, W L Alward, B E Nichols, et al.
Human Molecular Genetics|December 1, 1992
Genetic linkage of autosomal dominant neovascular inflammatory vitreoretinopathy to chromosome 11q13E M Stone, A E Kimura, J C Folk, et al.
Nature Genetics|May 1, 1993
Genetic linkage of familial open angle glaucoma to chromosome 1q21-q31V C Sheffield, E M Stone, W L Alward, et al.
Investigative Ophthalmology & Visual Science|September 28, 2000
Localization of MYOC transcripts in human eye and optic nerve by in situ hybridizationR E Swiderski, J L Ross, J H Fingert, et al.
American Journal of Ophthalmology|September 4, 1998
Relative afferent pupillary defects in patients with Leber hereditary optic neuropathy and unilateral visual lossD M Jacobson, E M Stone, N R Miller, et al.
Pageof 18

Showing results (101-110 of 174) with videos related to

Sort By:
Pageof 18
Ophthalmic Genetics|November 12, 1998
Rhodopsin C110Y mutation causes a type 2 autosomal dominant retinitis pigmentosaE Millá, E Héon, P A Grounauer, et al.
Nature Genetics|December 8, 1998
Allelic variation in ABCR associated with Stargardt disease but not age-related macular degenerationE M Stone, A R Webster, K Vandenburgh, et al.
Investigative Ophthalmology & Visual Science|August 1, 1996
Sub-retinal pigment epithelial deposits in a dominant late-onset retinal degenerationC A Kuntz, S G Jacobson, A V Cideciyan, et al.
Ophthalmology|October 1, 1992
Avellino corneal dystrophy. Clinical manifestations and natural historyE J Holland, S M Daya, E M Stone, et al.
American Journal of Ophthalmology|January 23, 1998
Autosomal dominant iris hypoplasia is caused by a mutation in the Rieger syndrome (RIEG/PITX2) geneW L Alward, E V Semina, J W Kalenak, et al.
Genome Research|September 1, 1996
Fine mapping of the autosomal dominant juvenile open angle glaucoma (GLC1A) region and evaluation of candidate genesS L Sunden, W L Alward, B E Nichols, et al.
Human Molecular Genetics|December 1, 1992
Genetic linkage of autosomal dominant neovascular inflammatory vitreoretinopathy to chromosome 11q13E M Stone, A E Kimura, J C Folk, et al.
Nature Genetics|May 1, 1993
Genetic linkage of familial open angle glaucoma to chromosome 1q21-q31V C Sheffield, E M Stone, W L Alward, et al.
Investigative Ophthalmology & Visual Science|September 28, 2000
Localization of MYOC transcripts in human eye and optic nerve by in situ hybridizationR E Swiderski, J L Ross, J H Fingert, et al.
American Journal of Ophthalmology|September 4, 1998
Relative afferent pupillary defects in patients with Leber hereditary optic neuropathy and unilateral visual lossD M Jacobson, E M Stone, N R Miller, et al.
Pageof 18