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

D Ducroq

Showing results (11-20 of 14) with videos related to

Pageof 2
Sort By:
You have reached the last page of results.This site can display upto 14 results.
American Journal of Ophthalmology|August 24, 1999
Age-related macular degeneration in grandparents of patients with Stargardt disease: genetic studyE H Souied, D Ducroq, S Gerber, et al.
American Journal of Human Genetics|March 26, 1999
Different functional outcome of RetGC1 and RPE65 gene mutations in Leber congenital amaurosisI Perrault, J M Rozet, I Ghazi, et al.
European Journal of Human Genetics : EJHG|August 31, 2001
Complete exon-intron structure of the RPGR-interacting protein (RPGRIP1) gene allows the identification of mutations underlying Leber congenital amaurosisS Gerber, I Perrault, S Hanein, et al.
Human Genetics|November 9, 2000
The photoreceptor cell-specific nuclear receptor gene (PNR) accounts for retinitis pigmentosa in the Crypto-Jews from Portugal (Marranos), survivors from the Spanish InquisitionS Gerber, J M Rozet, S I Takezawa, et al.
Pageof 2

Showing results (11-20 of 14) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 14 results.
American Journal of Ophthalmology|August 24, 1999
Age-related macular degeneration in grandparents of patients with Stargardt disease: genetic studyE H Souied, D Ducroq, S Gerber, et al.
American Journal of Human Genetics|March 26, 1999
Different functional outcome of RetGC1 and RPE65 gene mutations in Leber congenital amaurosisI Perrault, J M Rozet, I Ghazi, et al.
European Journal of Human Genetics : EJHG|August 31, 2001
Complete exon-intron structure of the RPGR-interacting protein (RPGRIP1) gene allows the identification of mutations underlying Leber congenital amaurosisS Gerber, I Perrault, S Hanein, et al.
Human Genetics|November 9, 2000
The photoreceptor cell-specific nuclear receptor gene (PNR) accounts for retinitis pigmentosa in the Crypto-Jews from Portugal (Marranos), survivors from the Spanish InquisitionS Gerber, J M Rozet, S I Takezawa, et al.
Pageof 2