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A T Moore

Showing results (81-90 of 148) with videos related to

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Human Molecular Genetics|January 1, 1997
A locus for autosomal dominant posterior polar cataract on chromosome 1pA C Ionides, V Berry, D S Mackay, et al.
The British Journal of Ophthalmology|March 20, 2004
Oligocone trichromacy: a rare and unusual cone dysfunction syndromeM Michaelides, G E Holder, K Bradshaw, et al.
Eye (London, England)|January 1, 1990
Ocular enlargement following infantile corneal opacificationJ M Twomey, A Gilvarry, M Restori, et al.
The British Journal of Ophthalmology|July 1, 1994
Carrier detection in X linked ocular albinism using linked DNA polymorphismsS J Charles, A T Moore, Y Zhang, et al.
Human Molecular Genetics|April 1, 1997
Localisation of a gene for dominant cone-rod dystrophy (CORD6) to chromosome 17pR E Kelsell, K Evans, C Y Gregory, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|October 26, 1999
Electrophysiological findings in dominant optic atrophy (DOA) linking to the OPA1 locus on chromosome 3q 28-qterG E Holder, M Votruba, A C Carter, et al.
Clinical Genetics|May 11, 2016
Advanced diagnostic genetic testing in inherited retinal disease: experience from a single tertiary referral centre in the UK National Health ServiceK N Khan, R Chana, N Ali, et al.
Journal of Medical Genetics|January 1, 1990
Linkage of internal minisatellite loci on chromosome 1 and exclusion of autosomal dominant retinitis pigmentosa proximal to rhesusC F Inglehearn, S S Papiha, M Jay, et al.
Journal of Medical Genetics|February 12, 2002
A locus for isolated cataract on human XpP J Francis, V Berry, A J Hardcastle, et al.
The British Journal of Ophthalmology|October 27, 2009
Cataract surgery and primary intraocular lens implantation in children < or = 2 years old in the UK and Ireland: finding of national surveysA L Solebo, I Russell-Eggitt, K K Nischal, et al.
Pageof 15

Showing results (81-90 of 148) with videos related to

Sort By:
Pageof 15
Human Molecular Genetics|January 1, 1997
A locus for autosomal dominant posterior polar cataract on chromosome 1pA C Ionides, V Berry, D S Mackay, et al.
The British Journal of Ophthalmology|March 20, 2004
Oligocone trichromacy: a rare and unusual cone dysfunction syndromeM Michaelides, G E Holder, K Bradshaw, et al.
Eye (London, England)|January 1, 1990
Ocular enlargement following infantile corneal opacificationJ M Twomey, A Gilvarry, M Restori, et al.
The British Journal of Ophthalmology|July 1, 1994
Carrier detection in X linked ocular albinism using linked DNA polymorphismsS J Charles, A T Moore, Y Zhang, et al.
Human Molecular Genetics|April 1, 1997
Localisation of a gene for dominant cone-rod dystrophy (CORD6) to chromosome 17pR E Kelsell, K Evans, C Y Gregory, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|October 26, 1999
Electrophysiological findings in dominant optic atrophy (DOA) linking to the OPA1 locus on chromosome 3q 28-qterG E Holder, M Votruba, A C Carter, et al.
Clinical Genetics|May 11, 2016
Advanced diagnostic genetic testing in inherited retinal disease: experience from a single tertiary referral centre in the UK National Health ServiceK N Khan, R Chana, N Ali, et al.
Journal of Medical Genetics|January 1, 1990
Linkage of internal minisatellite loci on chromosome 1 and exclusion of autosomal dominant retinitis pigmentosa proximal to rhesusC F Inglehearn, S S Papiha, M Jay, et al.
Journal of Medical Genetics|February 12, 2002
A locus for isolated cataract on human XpP J Francis, V Berry, A J Hardcastle, et al.
The British Journal of Ophthalmology|October 27, 2009
Cataract surgery and primary intraocular lens implantation in children < or = 2 years old in the UK and Ireland: finding of national surveysA L Solebo, I Russell-Eggitt, K K Nischal, et al.
Pageof 15