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 Meire

Showing results (31-40 of 54) with videos related to

Pageof 6
Sort By:
Ophthalmic Genetics|February 5, 2003
Corneal decompensation in a boy with Kearns-Sayre syndromeF Boonstra, I Claerhout, F Hol, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|October 1, 1990
Functional quantification of diaphanyT J Van den Berg, J K Ijspeert, P W de Waard, et al.
The British Journal of Ophthalmology|April 26, 2003
Corneal deposits after the topical use of ofloxacin in two children with vernal keratoconjunctivitisI Claerhout, Ph Kestelyn, F Meire, et al.
Bulletin De La Societe Belge D'Ophtalmologie|June 6, 2003
Psammomatoid ossifying fibroma of the ethmoidK Vandekerckhove, K Van den Abeele, C Van den Broecke, et al.
Bulletin De La Societe Belge D'Ophtalmologie|January 1, 1993
Treatment of long-term complications of toxoplasma chorioretinal scarsK Buys, I Casteels, R Vianna, et al.
Ophthalmic Paediatrics and Genetics|February 1, 1985
Dominant optic nerve atrophy with progressive hearing loss and chronic progressive external ophthalmoplegia (CPEO)F Meire, J J De Laey, S de Bie, et al.
American Journal of Medical Genetics|October 28, 1996
Fibrotic eye muscles, Axenfeld anomaly, flat face, and mild developmental retardation: a new example of the Chitty syndromeS G Van Daele, R N Van Coster, F Meire, et al.
Human Mutation|January 1, 1996
Three novel and two recurrent mutations of the Norrie disease gene in patients with Norrie syndromeS Fuchs, D van de Pol, U Beudt, et al.
Human Molecular Genetics|February 5, 1999
Missense mutations in the most ancient residues of the PAX6 paired domain underlie a spectrum of human congenital eye malformationsI Hanson, A Churchill, J Love, et al.
Clinical Genetics|May 1, 1996
Cohen syndrome: the clinical symptoms and stigmata at a young ageJ P Fryns, E Legius, K Devriendt, et al.
Pageof 6

Showing results (31-40 of 54) with videos related to

Sort By:
Pageof 6
Ophthalmic Genetics|February 5, 2003
Corneal decompensation in a boy with Kearns-Sayre syndromeF Boonstra, I Claerhout, F Hol, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|October 1, 1990
Functional quantification of diaphanyT J Van den Berg, J K Ijspeert, P W de Waard, et al.
The British Journal of Ophthalmology|April 26, 2003
Corneal deposits after the topical use of ofloxacin in two children with vernal keratoconjunctivitisI Claerhout, Ph Kestelyn, F Meire, et al.
Bulletin De La Societe Belge D'Ophtalmologie|June 6, 2003
Psammomatoid ossifying fibroma of the ethmoidK Vandekerckhove, K Van den Abeele, C Van den Broecke, et al.
Bulletin De La Societe Belge D'Ophtalmologie|January 1, 1993
Treatment of long-term complications of toxoplasma chorioretinal scarsK Buys, I Casteels, R Vianna, et al.
Ophthalmic Paediatrics and Genetics|February 1, 1985
Dominant optic nerve atrophy with progressive hearing loss and chronic progressive external ophthalmoplegia (CPEO)F Meire, J J De Laey, S de Bie, et al.
American Journal of Medical Genetics|October 28, 1996
Fibrotic eye muscles, Axenfeld anomaly, flat face, and mild developmental retardation: a new example of the Chitty syndromeS G Van Daele, R N Van Coster, F Meire, et al.
Human Mutation|January 1, 1996
Three novel and two recurrent mutations of the Norrie disease gene in patients with Norrie syndromeS Fuchs, D van de Pol, U Beudt, et al.
Human Molecular Genetics|February 5, 1999
Missense mutations in the most ancient residues of the PAX6 paired domain underlie a spectrum of human congenital eye malformationsI Hanson, A Churchill, J Love, et al.
Clinical Genetics|May 1, 1996
Cohen syndrome: the clinical symptoms and stigmata at a young ageJ P Fryns, E Legius, K Devriendt, et al.
Pageof 6