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Ophthalmic Genetics|March 17, 2022
Adherence and satisfaction in Argus II prosthesis users: a self determination theory modelMariam Khan, Kari Branham, Kanishka T Jayasundera, et al.Ophthalmic Genetics|January 3, 2001
A new association of congenital hydrocephalus, albinism, megalocornea, and retinal coloboma in a syndromic child: a clinical and genetic studyP Dubé, Der Kaloustian VM, S Demczuk, et al.Ophthalmic Genetics|January 3, 2001
Bilateral microphthalmos with colobomatous orbital cyst and de-novo balanced translocation t(3;5)M Kurbasic, F V Jones, L N CookOphthalmic Genetics|January 3, 2001
Ser186Pro mutation of RHO gene in a Spanish autosomal dominant retinitis pigmentosa (ADRP) familyM J Trujillo, B Garcia-Sandoval, I Lorda-Sanchez, et al.Ophthalmic Genetics|January 5, 2000
A family with autosomal dominant distal arthrogryposis multiplex congenita and brown syndromeL T Lobefalo, A T Mancini, M T Petitti, et al.Ophthalmic Genetics|October 16, 1999
Rhegmatogenous retinal detachment after treatment of retinoblastomaE H Bovey, A Fernandez-Ragaz, E Héon, et al.Ophthalmic Genetics|October 16, 1999
Secondary mutations of mitochondrial DNA in Japanese patients with Leber's hereditary optic neuropathyM Matsumoto, S Hayasaka, C Kadoi, et al.Ophthalmic Genetics|October 16, 1999
Agenesis of the corpus callosum in a child with Leber's congenital amaurosisH Kiratli, S TatlipinarOphthalmic Genetics|October 16, 1999
Circulating retinoblastoma cells in a patient with metastatic diseaseP Zubizarreta, G ChantadaOphthalmic Genetics|April 26, 2000
Microfibril abnormalities of the lens capsule in patients with Marfan syndrome and ectopia lentisE I Traboulsi, J A Whittum-Hudson, S H Mir, et al.Pageof 185