Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

A J Hardcastle

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

Pageof 4
Sort By:
American Journal of Human Genetics|February 1, 1996
Nomenclature for inherited diseases of the retinaC F Inglehearn, A J Hardcastle
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|June 2, 2016
Cone opsins, colour blindness and cone dystrophy: Genotype-phenotype correlationsJ C Gardner, M Michaelides, A J Hardcastle
Eye (London, England)|December 21, 2013
The pathogenesis of keratoconusA E Davidson, S Hayes, A J Hardcastle, et al.
Investigative Ophthalmology & Visual Science|August 1, 1997
Genomic organization of the human TIMP-1 gene. Investigation of a causative role in the pathogenesis of X-linked retinitis pigmentosa 2A J Hardcastle, D L Thiselton, M Nayudu, et al.
Eye (London, England)|December 11, 2012
Severe Meesmann's epithelial corneal dystrophy phenotype due to a missense mutation in the helix-initiation motif of keratin 12H Hassan, C Thaung, N D Ebenezer, et al.
Cytogenetics and Cell Genetics|October 12, 1999
Assignment of the neuronal cochaperone, HSJ1, to human chromosome bands 2q32-->q34 between D2S295 and D2S339 by in situ hybridization and somatic cell and radiation hybridsJ P Chapple, A J Hardcastle, U Kurzik-Dumke, et al.
Investigative Ophthalmology & Visual Science|January 7, 1998
Localization of CSNBX (CSNB4) between the retinitis pigmentosa loci RP2 and RP3 on proximal XpA J Hardcastle, Z K David-Gray, M Jay, et al.
Retina (Philadelphia, Pa.)|February 24, 2001
Optical coherence tomography and electrophysiology in X-linked juvenile retinoschisis associated with a novel mutation in the XLRS1 geneP E Stanga, N H Chong, A C Reck, et al.
Genomics|January 1, 1995
Genetic and physical mapping of five novel microsatellite markers on human Xp21.1-p11.22D L Thiselton, S Lindsay, S Kamakari, et al.
Human Mutation|March 29, 2000
Novel mutations of the RPGR gene in RP3 familiesI Zito, M B Gorin, C Plant, et al.
Pageof 4

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

Sort By:
Pageof 4
American Journal of Human Genetics|February 1, 1996
Nomenclature for inherited diseases of the retinaC F Inglehearn, A J Hardcastle
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|June 2, 2016
Cone opsins, colour blindness and cone dystrophy: Genotype-phenotype correlationsJ C Gardner, M Michaelides, A J Hardcastle
Eye (London, England)|December 21, 2013
The pathogenesis of keratoconusA E Davidson, S Hayes, A J Hardcastle, et al.
Investigative Ophthalmology & Visual Science|August 1, 1997
Genomic organization of the human TIMP-1 gene. Investigation of a causative role in the pathogenesis of X-linked retinitis pigmentosa 2A J Hardcastle, D L Thiselton, M Nayudu, et al.
Eye (London, England)|December 11, 2012
Severe Meesmann's epithelial corneal dystrophy phenotype due to a missense mutation in the helix-initiation motif of keratin 12H Hassan, C Thaung, N D Ebenezer, et al.
Cytogenetics and Cell Genetics|October 12, 1999
Assignment of the neuronal cochaperone, HSJ1, to human chromosome bands 2q32-->q34 between D2S295 and D2S339 by in situ hybridization and somatic cell and radiation hybridsJ P Chapple, A J Hardcastle, U Kurzik-Dumke, et al.
Investigative Ophthalmology & Visual Science|January 7, 1998
Localization of CSNBX (CSNB4) between the retinitis pigmentosa loci RP2 and RP3 on proximal XpA J Hardcastle, Z K David-Gray, M Jay, et al.
Retina (Philadelphia, Pa.)|February 24, 2001
Optical coherence tomography and electrophysiology in X-linked juvenile retinoschisis associated with a novel mutation in the XLRS1 geneP E Stanga, N H Chong, A C Reck, et al.
Genomics|January 1, 1995
Genetic and physical mapping of five novel microsatellite markers on human Xp21.1-p11.22D L Thiselton, S Lindsay, S Kamakari, et al.
Human Mutation|March 29, 2000
Novel mutations of the RPGR gene in RP3 familiesI Zito, M B Gorin, C Plant, et al.
Pageof 4