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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 study
A 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 19
M 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 expression
R 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 19q
K 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 Uganda
C 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 sunlight
J 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 loss
P J Francis, S Johnson, B Edmunds, et al.
Eye (London, England)
|
June 27, 2015
Diverse clinical phenotypes associated with a nonsense mutation in FAM161A
A M Rose, P Sergouniotis, G Alfano, et al.
Page
of 15
Search research articles
Search
Showing results (111-120 of 148) with videos related to
Sort By:
Page
of 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 study
A 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 19
M 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 expression
R 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 19q
K 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 Uganda
C 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 sunlight
J 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 loss
P J Francis, S Johnson, B Edmunds, et al.
Eye (London, England)
|
June 27, 2015
Diverse clinical phenotypes associated with a nonsense mutation in FAM161A
A M Rose, P Sergouniotis, G Alfano, et al.
Page
of 15