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

N Ducrey

Showing results (61-70 of 66) with videos related to

Pageof 7
Sort By:
You have reached the last page of results.This site can display upto 66 results.
Klinische Monatsblatter Fur Augenheilkunde|July 25, 1998
[Mutational screening of peripherin/RDS genes, rhodopsin and ROM-1 in 69 index cases with retinitis pigmentosa and other retinal dystrophies]E Millá, E Héon, B Piguet, et al.
The Journal of Cardiovascular Surgery|September 6, 2006
Clinical results of autologous infrainguinal revascularization using grafts originating distal to the femoral bifurcation in patients with mild inflow diseaseH Probst, F Saucy, M Dusmet, et al.
Investigative Ophthalmology & Visual Science|January 14, 2000
Genetic heterogeneity of the Coppock-like cataract: a mutation in CRYBB2 on chromosome 22q11.2D Gill, R Klose, F L Munier, et al.
Ophthalmic Genetics|November 12, 1998
Rhodopsin C110Y mutation causes a type 2 autosomal dominant retinitis pigmentosaE Millá, E Héon, P A Grounauer, et al.
Neuro-Chirurgie|March 23, 2010
[Orbitotemporal facial involvement in type 1 neurofibromatosis (NF1)]B Rilliet, B Pittet, D Montandon, et al.
The British Journal of Ophthalmology|May 5, 2006
Primary lymphoma of the lacrimal sac: an EORTC ophthalmic oncology task force studyL D Sjö, E Ralfkiaer, B R Juhl, et al.
Pageof 7

Showing results (61-70 of 66) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 66 results.
Klinische Monatsblatter Fur Augenheilkunde|July 25, 1998
[Mutational screening of peripherin/RDS genes, rhodopsin and ROM-1 in 69 index cases with retinitis pigmentosa and other retinal dystrophies]E Millá, E Héon, B Piguet, et al.
The Journal of Cardiovascular Surgery|September 6, 2006
Clinical results of autologous infrainguinal revascularization using grafts originating distal to the femoral bifurcation in patients with mild inflow diseaseH Probst, F Saucy, M Dusmet, et al.
Investigative Ophthalmology & Visual Science|January 14, 2000
Genetic heterogeneity of the Coppock-like cataract: a mutation in CRYBB2 on chromosome 22q11.2D Gill, R Klose, F L Munier, et al.
Ophthalmic Genetics|November 12, 1998
Rhodopsin C110Y mutation causes a type 2 autosomal dominant retinitis pigmentosaE Millá, E Héon, P A Grounauer, et al.
Neuro-Chirurgie|March 23, 2010
[Orbitotemporal facial involvement in type 1 neurofibromatosis (NF1)]B Rilliet, B Pittet, D Montandon, et al.
The British Journal of Ophthalmology|May 5, 2006
Primary lymphoma of the lacrimal sac: an EORTC ophthalmic oncology task force studyL D Sjö, E Ralfkiaer, B R Juhl, et al.
Pageof 7