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 G Aktan

Showing results (1-10 of 9) with videos related to

Pageof 1
Sort By:
Ophthalmic Surgery and Lasers|August 26, 1998
Krypton laser suture lysisS G Aktan, R M Mandelkorn
European Journal of Ophthalmology|July 1, 1995
Ophthalmic screening of school children in AnkaraM E Turaçli, S G Aktan, K Dürük
Ophthalmologica. Journal International D'Ophtalmologie. International Journal of Ophthalmology. Zeitschrift Fur Augenheilkunde|January 1, 1995
Gonioscopic evaluation of glaucoma patients after trabeculectomyM E Turaçh, S G Aktan, M Serhatli
Ophthalmologica. Journal International D'Ophtalmologie. International Journal of Ophthalmology. Zeitschrift Fur Augenheilkunde|October 27, 1998
Problems of chorioretinal venous anastomosis by laser for treatment of nonischemic central retinal vein occlusionS G Aktan, M Subaşi, H Akbatur, et al.
International Ophthalmology|September 1, 1992
Therapeutical and genetical aspects of congenital glaucomasM E Turaçli, S G Aktan, B S Sayli, et al.
Human Molecular Genetics|August 1, 1996
A second locus (GLC3B) for primary congenital glaucoma (Buphthalmos) maps to the 1p36 regionA N Akarsu, M E Turacli, S G Aktan, et al.
Genomics|November 20, 1995
Assignment of a locus (GLC3A) for primary congenital glaucoma (Buphthalmos) to 2p21 and evidence for genetic heterogeneityM Sarfarazi, A N Akarsu, A Hossain, et al.
American Journal of Medical Genetics|January 22, 1996
Exclusion of primary congenital glaucoma (buphthalmos) from two candidate regions of chromosome arm 6p and chromosome 11A N Akarsu, M E Turacli, S G Aktan, et al.
American Journal of Human Genetics|April 29, 1998
Sequence analysis and homology modeling suggest that primary congenital glaucoma on 2p21 results from mutations disrupting either the hinge region or the conserved core structures of cytochrome P4501B1I Stoilov, A N Akarsu, I Alozie, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Ophthalmic Surgery and Lasers|August 26, 1998
Krypton laser suture lysisS G Aktan, R M Mandelkorn
European Journal of Ophthalmology|July 1, 1995
Ophthalmic screening of school children in AnkaraM E Turaçli, S G Aktan, K Dürük
Ophthalmologica. Journal International D'Ophtalmologie. International Journal of Ophthalmology. Zeitschrift Fur Augenheilkunde|January 1, 1995
Gonioscopic evaluation of glaucoma patients after trabeculectomyM E Turaçh, S G Aktan, M Serhatli
Ophthalmologica. Journal International D'Ophtalmologie. International Journal of Ophthalmology. Zeitschrift Fur Augenheilkunde|October 27, 1998
Problems of chorioretinal venous anastomosis by laser for treatment of nonischemic central retinal vein occlusionS G Aktan, M Subaşi, H Akbatur, et al.
International Ophthalmology|September 1, 1992
Therapeutical and genetical aspects of congenital glaucomasM E Turaçli, S G Aktan, B S Sayli, et al.
Human Molecular Genetics|August 1, 1996
A second locus (GLC3B) for primary congenital glaucoma (Buphthalmos) maps to the 1p36 regionA N Akarsu, M E Turacli, S G Aktan, et al.
Genomics|November 20, 1995
Assignment of a locus (GLC3A) for primary congenital glaucoma (Buphthalmos) to 2p21 and evidence for genetic heterogeneityM Sarfarazi, A N Akarsu, A Hossain, et al.
American Journal of Medical Genetics|January 22, 1996
Exclusion of primary congenital glaucoma (buphthalmos) from two candidate regions of chromosome arm 6p and chromosome 11A N Akarsu, M E Turacli, S G Aktan, et al.
American Journal of Human Genetics|April 29, 1998
Sequence analysis and homology modeling suggest that primary congenital glaucoma on 2p21 results from mutations disrupting either the hinge region or the conserved core structures of cytochrome P4501B1I Stoilov, A N Akarsu, I Alozie, et al.
Pageof 1