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A T Moore

Showing results (91-100 of 148) with videos related to

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The Journal of Pediatrics|April 1, 1985
Tenosynovitis of the superior oblique muscle (Brown syndrome) associated with juvenile rheumatoid arthritisC M Roifman, S Lavi, A T Moore, et al.
The British Journal of Ophthalmology|January 25, 2005
A detailed study of the phenotype of an autosomal dominant cone-rod dystrophy (CORD7) associated with mutation in the gene for RIM1M Michaelides, G E Holder, D M Hunt, et al.
Journal of Medical Genetics|October 7, 2004
Identification of the gene for Nance-Horan syndrome (NHS)S P Brooks, N D Ebenezer, S Poopalasundaram, et al.
Eye (London, England)|April 16, 2011
Mizuo-Nakamura phenomenon in Oguchi disease due to a homozygous nonsense mutation in the SAG geneP I Sergouniotis, A E Davidson, K Sehmi, et al.
Eye (London, England)|May 23, 2015
Congenital high myopia and central macular atrophy: a report of 3 familiesS Hull, A Kalhoro, J Marr, et al.
Journal of Medical Genetics|November 1, 1996
Improved genetic mapping of X linked retinoschisisN D George, S J Payne, R M Bill, et al.
Eye (London, England)|October 21, 2000
Who should manage primary retinal detachments?M B Comer, D K Newman, N D George, et al.
Neuroradiology|April 20, 2000
MRI of the intraorbital optic nerve in patients with autosomal dominant optic atrophyM Votruba, S Leary, N Losseff, et al.
The British Journal of Ophthalmology|September 20, 2005
Temperature sensitive oculocutaneous albinism associated with missense changes in the tyrosinase geneT Wang, C T Waters, T Jakins, et al.
Journal of Medical Genetics|November 1, 1993
Genetic mapping of the Kallmann syndrome and X linked ocular albinism gene lociY Zhang, R McMahon, S J Charles, et al.
Pageof 15

Showing results (91-100 of 148) with videos related to

Sort By:
Pageof 15
The Journal of Pediatrics|April 1, 1985
Tenosynovitis of the superior oblique muscle (Brown syndrome) associated with juvenile rheumatoid arthritisC M Roifman, S Lavi, A T Moore, et al.
The British Journal of Ophthalmology|January 25, 2005
A detailed study of the phenotype of an autosomal dominant cone-rod dystrophy (CORD7) associated with mutation in the gene for RIM1M Michaelides, G E Holder, D M Hunt, et al.
Journal of Medical Genetics|October 7, 2004
Identification of the gene for Nance-Horan syndrome (NHS)S P Brooks, N D Ebenezer, S Poopalasundaram, et al.
Eye (London, England)|April 16, 2011
Mizuo-Nakamura phenomenon in Oguchi disease due to a homozygous nonsense mutation in the SAG geneP I Sergouniotis, A E Davidson, K Sehmi, et al.
Eye (London, England)|May 23, 2015
Congenital high myopia and central macular atrophy: a report of 3 familiesS Hull, A Kalhoro, J Marr, et al.
Journal of Medical Genetics|November 1, 1996
Improved genetic mapping of X linked retinoschisisN D George, S J Payne, R M Bill, et al.
Eye (London, England)|October 21, 2000
Who should manage primary retinal detachments?M B Comer, D K Newman, N D George, et al.
Neuroradiology|April 20, 2000
MRI of the intraorbital optic nerve in patients with autosomal dominant optic atrophyM Votruba, S Leary, N Losseff, et al.
The British Journal of Ophthalmology|September 20, 2005
Temperature sensitive oculocutaneous albinism associated with missense changes in the tyrosinase geneT Wang, C T Waters, T Jakins, et al.
Journal of Medical Genetics|November 1, 1993
Genetic mapping of the Kallmann syndrome and X linked ocular albinism gene lociY Zhang, R McMahon, S J Charles, et al.
Pageof 15