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

B Gorin

Showing results (91-100 of 175) with videos related to

Pageof 18
Sort By:
Investigative Ophthalmology & Visual Science|September 1, 1986
The gene for the major intrinsic protein (MIP) of the ocular lens is assigned to human chromosome 12cen-q14R S Sparkes, T Mohandas, C Heinzmann, et al.
Journal of Medical Genetics|June 17, 2003
A new genetic locus for X linked progressive cone-rod dystrophyR Jalkanen, F Y Demirci, H Tyynismaa, et al.
DNA Sequence : the Journal of DNA Sequencing and Mapping|June 27, 2003
Refinement of the physical location and the genomic characterization of the CRSP2 (EXLM1) gene on Xp11.4F Yesim Demirci, Juliane Ramser, Nicola J White, et al.
American Journal of Ophthalmology|March 1, 2005
Histopathologic study of X-linked cone-rod dystrophy (CORDX1) caused by a mutation in the RPGR exon ORF15F Yesim K Demirci, Nisha Gupta, Amy L Radak, et al.
Journal of Medical Genetics|April 4, 2000
Genetic heterogeneity of Usher syndrome type II: localisation to chromosome 5qS Pieke-Dahl, C G Möller, P M Kelley, et al.
Ophthalmology|April 1, 1988
Genetic linkage analysis of autosomal dominant congenital cataracts with lens-specific DNA probes and polymorphic phenotypic markersD J Barrett, R S Sparkes, M B Gorin, et al.
Ophthalmology|December 13, 2023
Consensus Guidelines for Ocular Surveillance of von Hippel-Lindau DiseaseAnthony B Daniels, Emmanuel Y Chang, Emily Y Chew, 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.
Genome Research|August 7, 2003
Detection and assignment of mutations and minihaplotypes in human DNA using peptide mass signature genotyping (PMSG): application to the human RDS/peripherin geneCheryl A Telmer, Adam C Retchless, Ashley D Kinsey, et al.
Cells|November 11, 2022
Membrane Attack Complex Mediates Retinal Pigment Epithelium Cell Death in Stargardt Macular DegenerationEunice Sze Yin Ng, Nermin Kady, Jane Hu, et al.
Pageof 18

Showing results (91-100 of 175) with videos related to

Sort By:
Pageof 18
Investigative Ophthalmology & Visual Science|September 1, 1986
The gene for the major intrinsic protein (MIP) of the ocular lens is assigned to human chromosome 12cen-q14R S Sparkes, T Mohandas, C Heinzmann, et al.
Journal of Medical Genetics|June 17, 2003
A new genetic locus for X linked progressive cone-rod dystrophyR Jalkanen, F Y Demirci, H Tyynismaa, et al.
DNA Sequence : the Journal of DNA Sequencing and Mapping|June 27, 2003
Refinement of the physical location and the genomic characterization of the CRSP2 (EXLM1) gene on Xp11.4F Yesim Demirci, Juliane Ramser, Nicola J White, et al.
American Journal of Ophthalmology|March 1, 2005
Histopathologic study of X-linked cone-rod dystrophy (CORDX1) caused by a mutation in the RPGR exon ORF15F Yesim K Demirci, Nisha Gupta, Amy L Radak, et al.
Journal of Medical Genetics|April 4, 2000
Genetic heterogeneity of Usher syndrome type II: localisation to chromosome 5qS Pieke-Dahl, C G Möller, P M Kelley, et al.
Ophthalmology|April 1, 1988
Genetic linkage analysis of autosomal dominant congenital cataracts with lens-specific DNA probes and polymorphic phenotypic markersD J Barrett, R S Sparkes, M B Gorin, et al.
Ophthalmology|December 13, 2023
Consensus Guidelines for Ocular Surveillance of von Hippel-Lindau DiseaseAnthony B Daniels, Emmanuel Y Chang, Emily Y Chew, 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.
Genome Research|August 7, 2003
Detection and assignment of mutations and minihaplotypes in human DNA using peptide mass signature genotyping (PMSG): application to the human RDS/peripherin geneCheryl A Telmer, Adam C Retchless, Ashley D Kinsey, et al.
Cells|November 11, 2022
Membrane Attack Complex Mediates Retinal Pigment Epithelium Cell Death in Stargardt Macular DegenerationEunice Sze Yin Ng, Nermin Kady, Jane Hu, et al.
Pageof 18