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Ophthalmic Genetics|February 5, 2013
Xq26.3 microdeletion in a male with Wildervanck SyndromeKhaled K Abu-Amero, Altaf A Kondkar, Ibrahim A Alorainy, et al.Ophthalmic Genetics|June 18, 2013
Childhood cone-rod dystrophy with macular cystic degeneration from recessive CRB1 mutationArif O Khan, Mohammed A Aldahmesh, Leen Abu-Safieh, et al.Ophthalmic Genetics|April 10, 2013
Choroidal neovascularization in Bardet-Biedl syndromeLeon D Charkoudian, David E Barañano, Jorge Fortun, et al.Ophthalmic Genetics|June 13, 2012
Microcornea with myopic chorioretinal atrophy, telecanthus and posteriorly-rotated ears: a distinct clinical syndromeArif O KhanOphthalmic Genetics|June 13, 2012
Neuro-ophthalmologic findings in humans with quadrupedal locomotionOzge Sarac, Suleyman Gulsuner, Yelda Yildiz-Tasci, et al.Ophthalmic Genetics|September 1, 1994
Angioid streaks associated with abetalipoproteinemiaM B Gorin, T O Paul, D J RaderOphthalmic Genetics|September 1, 1994
Macular dysplasia and pigmented paravenous retino-choroidal atrophyP Nucci, M P Manitto, A Piantanida, et al.Ophthalmic Genetics|March 23, 2002
Visual improvement in Leber congenital amaurosis and the CRX genotypeRobert K Koenekoop, Magali Loyer, Olga Dembinska, et al.Ophthalmic Genetics|June 1, 1997
Histopathological and immunohistochemical findings associated with a null mutation in the Norrie disease geneB Schroeder, L Hesse, W Brück, et al.Ophthalmic Genetics|June 1, 1997
Peroxisomal bifunctional enzyme deficiency with associated retinal findingsS A Al-Hazzaa, P T OzandPageof 185