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Ophthalmic Genetics|November 12, 2010
Microperimetry and OCT findings in female carriers of choroideremiaAzzrah Thobani, Anastasios Anastasakis, Gerald A FishmanOphthalmic Genetics|June 15, 2007
Gillespie syndrome: additional findings and parental consanguinityDaniela Varela Luquetti, Ruy Pires Oliveira-Sobrinho, Vera Lúcia Gil-da-Silva-LopesOphthalmic Genetics|June 15, 2007
Vision impairment with an interstitial deletion of the short arm of chromosome 8Rosalind M K Stewart, David C Assheton, Richard P Hagan, et al.Ophthalmic Genetics|November 9, 2011
Lack of association between polymorphisms in the prostaglandin F2α receptor and solute carrier organic anion transporter family 2A1 genes and intraocular pressure response to prostaglandin analogsCatherine A McCarty, Richard Berg, Richard Patchett, et al.Ophthalmic Genetics|January 11, 2012
Axenfeld-Rieger spectrum in a patient with 45,X Turner syndromeEbtesam Mohamed Abdalla, Karim Mahmoud NabilOphthalmic Genetics|December 17, 2011
Thirty-two years follow-up of X-linked juvenile retinoschisis in a Chinese patient with RS1 mutationFei Xu, Ruifang Sui, Fangtian DongOphthalmic Genetics|July 7, 2011
Strabismus, refractive errors and nystagmus in children and young adults with Down syndromeAntonela Ljubic, Vladimir Trajkovski, Branislav StankovicOphthalmic Genetics|October 25, 2011
Choroideremia: a review of general findings and pathogenesisRazek Georges Coussa, Elias I TraboulsiOphthalmic Genetics|June 29, 2011
Structural and functional measures of inner retinal integrity following visual acuity improvement in a patient with hereditary motor and sensory neuropathy type VISowjanya Gowrisankaran, Anastasios Anastasakis, Gerald A Fishman, et al.Ophthalmic Genetics|September 1, 1996
Septo-optic dysplasia associated with bilateral complex microphthalmosK Gündüz, I Günalp, I SaatçiPageof 185