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C Plant

Showing results (21-30 of 33) with videos related to

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Human Molecular Genetics|December 1, 1995
Linkage of congenital hereditary endothelial dystrophy to chromosome 20N M Toma, N D Ebenezer, C F Inglehearn, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|July 1, 1997
Assessment of the phenotypic range seen in Doyne honeycomb retinal dystrophyK Evans, C Y Gregory, S D Wijesuriya, et al.
Journal of Medical Genetics|October 3, 1999
Genetic analysis of the guanylate cyclase activator 1B (GUCA1B) gene in patients with autosomal dominant retinal dystrophiesA M Payne, S M Downes, D A Bessant, et al.
Human Mutation|June 22, 2000
Novel frameshift mutations in the RP2 gene and polymorphic variantsD L Thiselton, I Zito, C Plant, et al.
Journal of Medical Genetics|February 25, 1998
A linkage survey of 20 dominant retinitis pigmentosa families: frequencies of the nine known loci and evidence for further heterogeneityC F Inglehearn, E E Tarttelin, C Plant, et al.
Human Genetics|September 10, 1999
Identification of novel RPGR (retinitis pigmentosa GTPase regulator) mutations in a subset of X-linked retinitis pigmentosa families segregating with the RP3 locusI Zito, D L Thiselton, M B Gorin, et al.
American Journal of Human Genetics|March 26, 1999
Mutations in the RP2 gene cause disease in 10% of families with familial X-linked retinitis pigmentosa assessed in this studyA J Hardcastle, D L Thiselton, L Van Maldergem, et al.
Human Molecular Genetics|July 1, 1996
The gene responsible for autosomal dominant Doyne's honeycomb retinal dystrophy (DHRD) maps to chromosome 2p16C Y Gregory, K Evans, S D Wijesuriya, et al.
Human Genetics|March 10, 1999
Refined genetic and physical positioning of the gene for Doyne honeycomb retinal dystrophy (DHRD)S Kermani, K Gregory-Evans, E E Tarttelin, 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.
Pageof 4

Showing results (21-30 of 33) with videos related to

Sort By:
Pageof 4
Human Molecular Genetics|December 1, 1995
Linkage of congenital hereditary endothelial dystrophy to chromosome 20N M Toma, N D Ebenezer, C F Inglehearn, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|July 1, 1997
Assessment of the phenotypic range seen in Doyne honeycomb retinal dystrophyK Evans, C Y Gregory, S D Wijesuriya, et al.
Journal of Medical Genetics|October 3, 1999
Genetic analysis of the guanylate cyclase activator 1B (GUCA1B) gene in patients with autosomal dominant retinal dystrophiesA M Payne, S M Downes, D A Bessant, et al.
Human Mutation|June 22, 2000
Novel frameshift mutations in the RP2 gene and polymorphic variantsD L Thiselton, I Zito, C Plant, et al.
Journal of Medical Genetics|February 25, 1998
A linkage survey of 20 dominant retinitis pigmentosa families: frequencies of the nine known loci and evidence for further heterogeneityC F Inglehearn, E E Tarttelin, C Plant, et al.
Human Genetics|September 10, 1999
Identification of novel RPGR (retinitis pigmentosa GTPase regulator) mutations in a subset of X-linked retinitis pigmentosa families segregating with the RP3 locusI Zito, D L Thiselton, M B Gorin, et al.
American Journal of Human Genetics|March 26, 1999
Mutations in the RP2 gene cause disease in 10% of families with familial X-linked retinitis pigmentosa assessed in this studyA J Hardcastle, D L Thiselton, L Van Maldergem, et al.
Human Molecular Genetics|July 1, 1996
The gene responsible for autosomal dominant Doyne's honeycomb retinal dystrophy (DHRD) maps to chromosome 2p16C Y Gregory, K Evans, S D Wijesuriya, et al.
Human Genetics|March 10, 1999
Refined genetic and physical positioning of the gene for Doyne honeycomb retinal dystrophy (DHRD)S Kermani, K Gregory-Evans, E E Tarttelin, 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.
Pageof 4