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Ophthalmic Genetics|August 23, 2017
Association of catalase polymorphisms with primary open-angle glaucoma in a Chinese populationBo Gong, Yi Shi, Chao Qu, et al.Ophthalmic Genetics|January 25, 2023
Biochemical measures of ovarian function in female survivors of retinoblastoma treated with intra-arterial melphalan: an initial reportPriya H Marathe, Ira J Dunkel, Jasmine H Francis, et al.Ophthalmic Genetics|March 23, 2001
Evaluation of RLBP1 in 50 autosomal recessive retinitis pigmentosa and 4 retinitis punctata albescens Spanish familiesS Bernal, M Calaf, A Adan, et al.Ophthalmic Genetics|March 23, 2001
Phenotype associated with an R120X nonsense mutation in the RP2 gene in a Japanese family with X-linked retinitis pigmentosaY Mashima, M Saga, K Akeo, et al.Ophthalmic Genetics|August 21, 2002
Electroretinographic changes in the inner retinal layers of the retained eyes of patients with sporadic unilateral retinoblastomaWojciech Lubiński, Stanisław Zajaczek, Zbigniew Sych, et al.Ophthalmic Genetics|August 21, 2002
Identification of a novel VMD2 mutation in Japanese patients with Best diseaseYasuo Yanagi, Hisaki Sekine, Mikiro MoriOphthalmic Genetics|September 27, 2002
Electroretinographic findings in Duchenne/Becker muscular dystrophy and correlation with genotypeAyfer Ulgenalp, F Hakan Oner, Meltem F Söylev, et al.Ophthalmic Genetics|September 27, 2002
A case of Moebius syndrome in association with Klinefelter syndromePatrick C Yeh, Michael A KippOphthalmic Genetics|September 27, 2002
Confirmation of the 14568 mutation in the mitochondrial ND6 gene as causative in Leber's hereditary optic neuropathySascha Fauser, Beate Leo-Kottler, Dorothea Besch, et al.Ophthalmic Genetics|March 23, 2001
Further delineation of the facial 13q14 deletion syndrome in 13 retinoblastoma patientsR I Bojinova, D F Schorderet, M C Addor, et al.Pageof 185