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Ophthalmic Genetics|March 1, 1997
Refinement of the locus for autosomal dominant juvenile optic atrophy to a 2 cM region on 3q28D Stoilova, A Child, S P Desai, et al.Ophthalmic Genetics|March 1, 1997
The ocular phenotype of the Bardet-Biedl syndrome. Comparison to non-syndromic retinitis pigmentosaA Iannaccone, G De Propris, S Roncati, et al.Ophthalmic Genetics|March 1, 1997
Second primary tumors in patients with retinoblastoma. A review of the literatureA C Moll, S M Imhof, L M Bouter, et al.Ophthalmic Genetics|March 1, 1997
Bilateral megalocornea with unilateral lens subluxationA O Saatci, M Söylev, S Kavukçu, et al.Ophthalmic Genetics|March 1, 1997
Spontaneous corneal rupture in Noonan syndrome. A case reportY K Au, W P Collins, J S Patel, et al.Ophthalmic Genetics|December 29, 2007
Pseudo-vitelliform macular detachment and cuticular drusen: exclusion of 6 candidate genesIrene A Barbazetto, Nicolas A Yannuzzi, Christina M Klais, et al.Ophthalmic Genetics|December 29, 2007
Chorioretinopathy and microcephaly with normal developmentHoda Ahmadi, Yasmin S BradfieldOphthalmic Genetics|March 27, 2014
Congenital hypothyroidism in Rieger SyndromeNurgül Örnek, Reyhan Oğurel, Kemal ÖrnekOphthalmic Genetics|April 11, 2012
Ocular anomalies in an infant with Klinefelter SyndromeAlexander T Juhn, Naeem U Nabi, Alex V LevinPageof 185