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A T Moore

Showing results (131-140 of 148) with videos related to

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Eye (London, England)|January 21, 2012
Angioid streaks with severe macular dysfunction and generalised retinal involvement due to a homozygous duplication in the ABCC6 geneM H Tan, O M Vanakker, H V Tran, et al.
Human Molecular Genetics|September 1, 1995
Localization of the gene for progressive bifocal chorioretinal atrophy (PBCRA) to chromosome 6qR E Kelsell, B F Godley, K Evans, et al.
The British Journal of Ophthalmology|January 30, 1999
Phenotype of a British North Carolina macular dystrophy family linked to chromosome 6qM B Reichel, R E Kelsell, J Fan, et al.
Human Molecular Genetics|June 1, 1994
Molecular genetic analysis of the 3p- syndromeM E Phipps, F Latif, A Prowse, et al.
The British Journal of Ophthalmology|November 12, 2003
Genotype-phenotype correlation in British families with X linked congenital stationary night blindnessL E Allen, I Zito, K Bradshaw, et al.
Nature Genetics|May 1, 1993
A new locus for autosomal dominant retinitis pigmentosa on chromosome 7pC F Inglehearn, S A Carter, T J Keen, et al.
Human Molecular Genetics|March 16, 2004
Characterization of the G91del CRYBA1/3-crystallin protein: a cause of human inherited cataractM A Reddy, O A Bateman, C Chakarova, et al.
Journal of Medical Genetics|August 1, 1993
Evaluation of molecular genetic diagnosis in the management of familial adenomatous polyposis coli: a population based studyE R Maher, D E Barton, R Slatter, et al.
Human Molecular Genetics|June 9, 1998
Mutations in the retinal guanylate cyclase (RETGC-1) gene in dominant cone-rod dystrophyR E Kelsell, K Gregory-Evans, A M Payne, et al.
American Journal of Human Genetics|June 23, 1998
Localization of a gene (CORD7) for a dominant cone-rod dystrophy to chromosome 6qR E Kelsell, K Gregory-Evans, C Y Gregory-Evans, et al.
Pageof 15

Showing results (131-140 of 148) with videos related to

Sort By:
Pageof 15
Eye (London, England)|January 21, 2012
Angioid streaks with severe macular dysfunction and generalised retinal involvement due to a homozygous duplication in the ABCC6 geneM H Tan, O M Vanakker, H V Tran, et al.
Human Molecular Genetics|September 1, 1995
Localization of the gene for progressive bifocal chorioretinal atrophy (PBCRA) to chromosome 6qR E Kelsell, B F Godley, K Evans, et al.
The British Journal of Ophthalmology|January 30, 1999
Phenotype of a British North Carolina macular dystrophy family linked to chromosome 6qM B Reichel, R E Kelsell, J Fan, et al.
Human Molecular Genetics|June 1, 1994
Molecular genetic analysis of the 3p- syndromeM E Phipps, F Latif, A Prowse, et al.
The British Journal of Ophthalmology|November 12, 2003
Genotype-phenotype correlation in British families with X linked congenital stationary night blindnessL E Allen, I Zito, K Bradshaw, et al.
Nature Genetics|May 1, 1993
A new locus for autosomal dominant retinitis pigmentosa on chromosome 7pC F Inglehearn, S A Carter, T J Keen, et al.
Human Molecular Genetics|March 16, 2004
Characterization of the G91del CRYBA1/3-crystallin protein: a cause of human inherited cataractM A Reddy, O A Bateman, C Chakarova, et al.
Journal of Medical Genetics|August 1, 1993
Evaluation of molecular genetic diagnosis in the management of familial adenomatous polyposis coli: a population based studyE R Maher, D E Barton, R Slatter, et al.
Human Molecular Genetics|June 9, 1998
Mutations in the retinal guanylate cyclase (RETGC-1) gene in dominant cone-rod dystrophyR E Kelsell, K Gregory-Evans, A M Payne, et al.
American Journal of Human Genetics|June 23, 1998
Localization of a gene (CORD7) for a dominant cone-rod dystrophy to chromosome 6qR E Kelsell, K Gregory-Evans, C Y Gregory-Evans, et al.
Pageof 15