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Human Molecular Genetics
|
January 1, 1997
A locus for autosomal dominant posterior polar cataract on chromosome 1p
A 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 syndrome
M Michaelides, G E Holder, K Bradshaw, et al.
Eye (London, England)
|
January 1, 1990
Ocular enlargement following infantile corneal opacification
J 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 polymorphisms
S 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 17p
R 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-qter
G 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 Service
K 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 rhesus
C F Inglehearn, S S Papiha, M Jay, et al.
Journal of Medical Genetics
|
February 12, 2002
A locus for isolated cataract on human Xp
P 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 surveys
A L Solebo, I Russell-Eggitt, K K Nischal, et al.
Page
of 15
Search research articles
Search
Showing results (81-90 of 148) with videos related to
Sort By:
Page
of 15
Human Molecular Genetics
|
January 1, 1997
A locus for autosomal dominant posterior polar cataract on chromosome 1p
A 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 syndrome
M Michaelides, G E Holder, K Bradshaw, et al.
Eye (London, England)
|
January 1, 1990
Ocular enlargement following infantile corneal opacification
J 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 polymorphisms
S 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 17p
R 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-qter
G 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 Service
K 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 rhesus
C F Inglehearn, S S Papiha, M Jay, et al.
Journal of Medical Genetics
|
February 12, 2002
A locus for isolated cataract on human Xp
P 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 surveys
A L Solebo, I Russell-Eggitt, K K Nischal, et al.
Page
of 15