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G C Black

Showing results (1-10 of 32) with videos related to

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The British Journal of Ophthalmology|December 6, 2001
Genetic testing--swings and roundabouts: a view from the United KingdomG C Black, D Donnai
Molecular Genetic Medicine|January 1, 1994
Molecular genetics of blindnessG C Black, I W Craig
Primary Care|September 1, 1985
Health risk appraisal in primary careG C Black, A L Ashton
Eye (London, England)|November 27, 2019
The integration of genomics into clinical ophthalmic services in the UKG C Black, C MacEwen, A J Lotery
The British Journal of Ophthalmology|October 1, 1996
Leber's hereditary optic neuropathy: heteroplasmy is likely to be significant in the expression of LHON in families with the 3460 ND1 mutationG C Black, K Morten, A Laborde, et al.
Lancet (London, England)|October 7, 2000
Somatic mutation in MECP2 as a non-fatal neurodevelopmental disorder in malesJ Clayton-Smith, P Watson, S Ramsden, et al.
The British Journal of Ophthalmology|October 27, 1999
Ophthalmology in the post-genomic eraG C Black, M E Boulton, P N Bishop, et al.
Eye (London, England)|March 22, 2008
A novel peripherin/RDS mutation resulting in a retinal dystrophy with phenotypic variationT S Kalyanasundaram, G C Black, J O'Sullivan, et al.
The American Journal of Psychiatry|December 1, 1974
Psychiatry peer review: the Ohio systemR R Miller, G C Black, P Y Ertel, et al.
Nucleic Acids Research|February 11, 1991
Dinucleotide repeat polymorphism at the MAOA locusG C Black, Z Y Chen, I W Craig, et al.
Pageof 4

Showing results (1-10 of 32) with videos related to

Sort By:
Pageof 4
The British Journal of Ophthalmology|December 6, 2001
Genetic testing--swings and roundabouts: a view from the United KingdomG C Black, D Donnai
Molecular Genetic Medicine|January 1, 1994
Molecular genetics of blindnessG C Black, I W Craig
Primary Care|September 1, 1985
Health risk appraisal in primary careG C Black, A L Ashton
Eye (London, England)|November 27, 2019
The integration of genomics into clinical ophthalmic services in the UKG C Black, C MacEwen, A J Lotery
The British Journal of Ophthalmology|October 1, 1996
Leber's hereditary optic neuropathy: heteroplasmy is likely to be significant in the expression of LHON in families with the 3460 ND1 mutationG C Black, K Morten, A Laborde, et al.
Lancet (London, England)|October 7, 2000
Somatic mutation in MECP2 as a non-fatal neurodevelopmental disorder in malesJ Clayton-Smith, P Watson, S Ramsden, et al.
The British Journal of Ophthalmology|October 27, 1999
Ophthalmology in the post-genomic eraG C Black, M E Boulton, P N Bishop, et al.
Eye (London, England)|March 22, 2008
A novel peripherin/RDS mutation resulting in a retinal dystrophy with phenotypic variationT S Kalyanasundaram, G C Black, J O'Sullivan, et al.
The American Journal of Psychiatry|December 1, 1974
Psychiatry peer review: the Ohio systemR R Miller, G C Black, P Y Ertel, et al.
Nucleic Acids Research|February 11, 1991
Dinucleotide repeat polymorphism at the MAOA locusG C Black, Z Y Chen, I W Craig, et al.
Pageof 4