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

F L Munier

Showing results (51-60 of 59) with videos related to

Pageof 6
Sort By:
You have reached the last page of results.This site can display upto 59 results.
American Journal of Human Genetics|September 23, 2000
Genetic linkage of Bietti crystallin corneoretinal dystrophy to chromosome 4q35X Jiao, F L Munier, F Iwata, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|May 18, 2001
Variation of codons 1961 and 2177 of the Stargardt disease gene is not associated with age-related macular degenerationR H Guymer, E Héon, A J Lotery, et al.
Investigative Ophthalmology & Visual Science|September 28, 2000
Ultrastructural and molecular analysis of Bowman's layer corneal dystrophies: an epithelial origin?A E Ridgway, S Akhtar, F L Munier, et al.
Investigative Ophthalmology & Visual Science|May 8, 2000
Allelic variation in the VMD2 gene in best disease and age-related macular degenerationA J Lotery, F L Munier, G A Fishman, et al.
American Journal of Human Genetics|April 16, 1998
Mutation hot spots in 5q31-linked corneal dystrophiesE Korvatska, F L Munier, A Djemaï, et al.
Human Mutation|March 10, 2001
Identification of novel VMD2 gene mutations in patients with best vitelliform macular dystrophyD Marchant, K Gogat, S Boutboul, et al.
Nature Genetics|June 16, 1999
A single EFEMP1 mutation associated with both Malattia Leventinese and Doyne honeycomb retinal dystrophyE M Stone, A J Lotery, F L Munier, et al.
Human Molecular Genetics|November 2, 2001
Missense mutations in COL8A2, the gene encoding the alpha2 chain of type VIII collagen, cause two forms of corneal endothelial dystrophyS Biswas, F L Munier, J Yardley, et al.
Klinische Monatsblatter Fur Augenheilkunde|February 4, 2011
[The IC3D classification of the corneal dystrophies]J S Weiss, H U Møller, W Lisch, et al.
Pageof 6

Showing results (51-60 of 59) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 59 results.
American Journal of Human Genetics|September 23, 2000
Genetic linkage of Bietti crystallin corneoretinal dystrophy to chromosome 4q35X Jiao, F L Munier, F Iwata, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|May 18, 2001
Variation of codons 1961 and 2177 of the Stargardt disease gene is not associated with age-related macular degenerationR H Guymer, E Héon, A J Lotery, et al.
Investigative Ophthalmology & Visual Science|September 28, 2000
Ultrastructural and molecular analysis of Bowman's layer corneal dystrophies: an epithelial origin?A E Ridgway, S Akhtar, F L Munier, et al.
Investigative Ophthalmology & Visual Science|May 8, 2000
Allelic variation in the VMD2 gene in best disease and age-related macular degenerationA J Lotery, F L Munier, G A Fishman, et al.
American Journal of Human Genetics|April 16, 1998
Mutation hot spots in 5q31-linked corneal dystrophiesE Korvatska, F L Munier, A Djemaï, et al.
Human Mutation|March 10, 2001
Identification of novel VMD2 gene mutations in patients with best vitelliform macular dystrophyD Marchant, K Gogat, S Boutboul, et al.
Nature Genetics|June 16, 1999
A single EFEMP1 mutation associated with both Malattia Leventinese and Doyne honeycomb retinal dystrophyE M Stone, A J Lotery, F L Munier, et al.
Human Molecular Genetics|November 2, 2001
Missense mutations in COL8A2, the gene encoding the alpha2 chain of type VIII collagen, cause two forms of corneal endothelial dystrophyS Biswas, F L Munier, J Yardley, et al.
Klinische Monatsblatter Fur Augenheilkunde|February 4, 2011
[The IC3D classification of the corneal dystrophies]J S Weiss, H U Møller, W Lisch, et al.
Pageof 6