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Ophthalmic Genetics|April 23, 2011
Horizontal gaze palsy and progressive scoliosis without ROBO3 mutationsKhaled K Abu-Amero, Flavio Faletra, Paolo Gasparini, et al.Ophthalmic Genetics|March 23, 2011
The relationship between angiotensin converting enzyme insertion/deletion polymorphism and age-related macular degenerationBaşak Uçer, Ozcan Kayıkçıoğlu, Göktuğ Seymenoğlu, et al.Ophthalmic Genetics|March 23, 2011
Retinal dystrophy in the oculo-auricular syndrome due to HMX1 mutationV Vaclavik, D F Schorderet, F-X Borruat, et al.Ophthalmic Genetics|December 23, 2010
RPGR: role in the photoreceptor cilium, human retinal disease, and gene therapyJutta Hosch, Birgit Lorenz, Knut StiegerOphthalmic Genetics|December 23, 2010
Ocular manifestations in hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber disease): a case-seriesMichele Rinaldi, Elisabetta Buscarini, Cesare Danesino, et al.Ophthalmic Genetics|January 4, 2011
Morphological and functional changes in multifocal vitelliform retinopathy and biallelic mutations in BEST1Elisabeth Wittström, Sara Ekvall, Patrik Schatz, et al.Ophthalmic Genetics|March 4, 2011
Clinical presentation and outcome of retinoblastoma among children treated at the National Cancer Institute (NCI) in Gezira, Sudan: a single Institution experienceAmel A E Ali, Sara M A Elsheikh, Ahmed Elhaj, et al.Ophthalmic Genetics|February 24, 2011
Conditions that can be mistaken as early childhood glaucomaArif O KhanOphthalmic Genetics|November 12, 2010
Assessing mitochondrial DNA nucleotide changes in spontaneous optic neuropathiesThomas M Bosley, Khaled K Abu-AmeroOphthalmic Genetics|November 12, 2010
Choroideremia in a woman with ectodermal dysplasia and complex translocations involving chromosomes X, 1, and 3Krishna Mukkamala, Ronald C Gentile, Judith Willner, et al.Pageof 185