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

S M Downes

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

Pageof 3
Sort By:
You have reached the last page of results.This site can display upto 30 results.
Ophthalmology|May 31, 2001
Polypoidal choroidal vasculopathy and central serous chorioretinopathyR M Ahuja, S M Downes, P E Stanga, 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.
International Ophthalmology|April 12, 2002
Comparison of optical coherence tomography and fluorescein angiography in assessing macular edema in retinal dystrophies: preliminary resultsP E Stanga, S M Downes, R M Ahuja, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|February 7, 2001
Autosomal dominant cone and cone-rod dystrophy with mutations in the guanylate cyclase activator 1A gene-encoding guanylate cyclase activating protein-1S M Downes, G E Holder, F W Fitzke, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|October 26, 1999
Clinical features of codon 172 RDS macular dystrophy: similar phenotype in 12 familiesS M Downes, F W Fitzke, G E Holder, et al.
Human Molecular Genetics|March 21, 1998
A mutation in guanylate cyclase activator 1A (GUCA1A) in an autosomal dominant cone dystrophy pedigree mapping to a new locus on chromosome 6p21.1A M Payne, S M Downes, D A Bessant, et al.
Journal of Medical Genetics|September 22, 2001
Clustering and frequency of mutations in the retinal guanylate cyclase (GUCY2D) gene in patients with dominant cone-rod dystrophiesA M Payne, A G Morris, S M Downes, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 16, 2001
Autosomal dominant cone-rod dystrophy with mutations in the guanylate cyclase 2D gene encoding retinal guanylate cyclase-1S M Downes, A M Payne, R E Kelsell, et al.
Journal of Medical Genetics|August 16, 2003
RPGR mutation associated with retinitis pigmentosa, impaired hearing, and sinorespiratory infectionsI Zito, S M Downes, R J Patel, et al.
Ophthalmology|January 27, 2000
Autosomal dominant cone-rod retinal dystrophy (CORD6) from heterozygous mutation of GUCY2D, which encodes retinal guanylate cyclaseK Gregory-Evans, R E Kelsell, C Y Gregory-Evans, et al.
Pageof 3

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

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 30 results.
Ophthalmology|May 31, 2001
Polypoidal choroidal vasculopathy and central serous chorioretinopathyR M Ahuja, S M Downes, P E Stanga, 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.
International Ophthalmology|April 12, 2002
Comparison of optical coherence tomography and fluorescein angiography in assessing macular edema in retinal dystrophies: preliminary resultsP E Stanga, S M Downes, R M Ahuja, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|February 7, 2001
Autosomal dominant cone and cone-rod dystrophy with mutations in the guanylate cyclase activator 1A gene-encoding guanylate cyclase activating protein-1S M Downes, G E Holder, F W Fitzke, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|October 26, 1999
Clinical features of codon 172 RDS macular dystrophy: similar phenotype in 12 familiesS M Downes, F W Fitzke, G E Holder, et al.
Human Molecular Genetics|March 21, 1998
A mutation in guanylate cyclase activator 1A (GUCA1A) in an autosomal dominant cone dystrophy pedigree mapping to a new locus on chromosome 6p21.1A M Payne, S M Downes, D A Bessant, et al.
Journal of Medical Genetics|September 22, 2001
Clustering and frequency of mutations in the retinal guanylate cyclase (GUCY2D) gene in patients with dominant cone-rod dystrophiesA M Payne, A G Morris, S M Downes, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 16, 2001
Autosomal dominant cone-rod dystrophy with mutations in the guanylate cyclase 2D gene encoding retinal guanylate cyclase-1S M Downes, A M Payne, R E Kelsell, et al.
Journal of Medical Genetics|August 16, 2003
RPGR mutation associated with retinitis pigmentosa, impaired hearing, and sinorespiratory infectionsI Zito, S M Downes, R J Patel, et al.
Ophthalmology|January 27, 2000
Autosomal dominant cone-rod retinal dystrophy (CORD6) from heterozygous mutation of GUCY2D, which encodes retinal guanylate cyclaseK Gregory-Evans, R E Kelsell, C Y Gregory-Evans, et al.
Pageof 3