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A T Moore

Showing results (111-120 of 148) with videos related to

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The British Journal of Ophthalmology|November 12, 2003
Cone dystrophy phenotype associated with a frameshift mutation (M280fsX291) in the alpha-subunit of cone specific transducin (GNAT2)M Michaelides, I A Aligianis, G E Holder, et al.
The British Journal of Ophthalmology|August 1, 1993
Autosomal dominant retinitis pigmentosa with apparent incomplete penetrance: a clinical, electrophysiological, psychophysical, and molecular genetic studyA T Moore, F Fitzke, M Jay, et al.
Human Molecular Genetics|February 1, 1994
Identification of a sixth locus for autosomal dominant retinitis pigmentosa on chromosome 19M al-Maghtheh, C F Inglehearn, T J Keen, et al.
The British Journal of Ophthalmology|January 1, 1995
Autosomal dominant retinitis pigmentosa mapping to chromosome 7p exhibits variable expressionR Y Kim, F W Fitzke, A T Moore, et al.
The British Journal of Ophthalmology|September 1, 1995
Bimodal expressivity in dominant retinitis pigmentosa genetically linked to chromosome 19qK Evans, M al-Maghtheh, F W Fitzke, et al.
AIDS (London, England)|August 1, 1988
Risk factors for the spread of AIDS in rural Africa: evidence from a comparative seroepidemiological survey of AIDS, hepatitis B and syphilis in southwestern UgandaC P Hudson, A J Hennis, P Kataaha, et al.
The British Journal of Ophthalmology|February 22, 2005
A detailed phenotypic study of "cone dystrophy with supernormal rod ERG"M Michaelides, G E Holder, A R Webster, et al.
The British Journal of Ophthalmology|December 20, 2005
Age related macular degeneration and sun exposure, iris colour, and skin sensitivity to sunlightJ C Khan, H Shahid, D A Thurlby, et al.
The British Journal of Ophthalmology|June 19, 2003
Genetic linkage analysis of a novel syndrome comprising North Carolina-like macular dystrophy and progressive sensorineural hearing lossP J Francis, S Johnson, B Edmunds, et al.
Eye (London, England)|June 27, 2015
Diverse clinical phenotypes associated with a nonsense mutation in FAM161AA M Rose, P Sergouniotis, G Alfano, et al.
Pageof 15

Showing results (111-120 of 148) with videos related to

Sort By:
Pageof 15
The British Journal of Ophthalmology|November 12, 2003
Cone dystrophy phenotype associated with a frameshift mutation (M280fsX291) in the alpha-subunit of cone specific transducin (GNAT2)M Michaelides, I A Aligianis, G E Holder, et al.
The British Journal of Ophthalmology|August 1, 1993
Autosomal dominant retinitis pigmentosa with apparent incomplete penetrance: a clinical, electrophysiological, psychophysical, and molecular genetic studyA T Moore, F Fitzke, M Jay, et al.
Human Molecular Genetics|February 1, 1994
Identification of a sixth locus for autosomal dominant retinitis pigmentosa on chromosome 19M al-Maghtheh, C F Inglehearn, T J Keen, et al.
The British Journal of Ophthalmology|January 1, 1995
Autosomal dominant retinitis pigmentosa mapping to chromosome 7p exhibits variable expressionR Y Kim, F W Fitzke, A T Moore, et al.
The British Journal of Ophthalmology|September 1, 1995
Bimodal expressivity in dominant retinitis pigmentosa genetically linked to chromosome 19qK Evans, M al-Maghtheh, F W Fitzke, et al.
AIDS (London, England)|August 1, 1988
Risk factors for the spread of AIDS in rural Africa: evidence from a comparative seroepidemiological survey of AIDS, hepatitis B and syphilis in southwestern UgandaC P Hudson, A J Hennis, P Kataaha, et al.
The British Journal of Ophthalmology|February 22, 2005
A detailed phenotypic study of "cone dystrophy with supernormal rod ERG"M Michaelides, G E Holder, A R Webster, et al.
The British Journal of Ophthalmology|December 20, 2005
Age related macular degeneration and sun exposure, iris colour, and skin sensitivity to sunlightJ C Khan, H Shahid, D A Thurlby, et al.
The British Journal of Ophthalmology|June 19, 2003
Genetic linkage analysis of a novel syndrome comprising North Carolina-like macular dystrophy and progressive sensorineural hearing lossP J Francis, S Johnson, B Edmunds, et al.
Eye (London, England)|June 27, 2015
Diverse clinical phenotypes associated with a nonsense mutation in FAM161AA M Rose, P Sergouniotis, G Alfano, et al.
Pageof 15