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Ophthalmic Genetics|February 19, 2016
OR2W3 sequence variants are unlikely to cause inherited retinal diseasesDror Sharon, Adva Kimchi, Carlo RivoltaOphthalmic Genetics|February 20, 2016
Intraretinal cystoid spaces in a patient with retinitis pigmentosa due to mutation in the MAK geneYu-Hung Lai, Jenina E Capasso, Richard Kaiser, et al.Ophthalmic Genetics|February 20, 2016
Macular cystoid spaces in patients with retinal dystrophyMichelle D Lingao, Anuradha Ganesh, Arcot S Karthikeyan, et al.Ophthalmic Genetics|February 18, 2016
Phenotypic observations in "hypotrichosis with juvenile macular dystrophy" (recessive CDH3 mutations)Arif O Khan, Hanno J BolzOphthalmic Genetics|October 21, 2017
New pathogenic variant in the FGF10 gene in the agenesis of lacrimal and salivary gland syndrome: Ophthalmological and genetic studyMaria Jesus Rodrigo, Miriam Idoipe, Silvia Izquierdo, et al.Ophthalmic Genetics|July 26, 2022
MFRP variant results in nanophthalmos, retinitis pigmentosa, variability in foveal avascular zoneClaire Vanden Heuvel, Breanna Aldred, Tyler Boulter, et al.Ophthalmic Genetics|July 25, 2022
OCT imaging of macular cysts and treatment response with nepafenac in mucopolysaccharidosis type 1Aslıhan Yılmaz Çebi, Mustafa HepokurOphthalmic Genetics|January 14, 2017
Association of retinal vein occlusion, homocysteine, and the thrombophilic mutations in a Turkish population: A case-control studyMehmet Talay Koylu, Murat Kucukevcilioglu, Fazil Cuneyt Erdurman, et al.Ophthalmic Genetics|January 14, 2017
Elderly onset vitreous opacities as the initial manifestation in hereditary transthyretin (ATTR Val30Met) carriesKyoko Ishida, Takashi Nishida, Yusuke Niimi, et al.Ophthalmic Genetics|January 14, 2017
A novel homozygous variant in the SMOC1 gene underlying Waardenburg anophthalmia syndromeAsmat Ullah, Muhammad Umair, Farooq Ahmad, et al.Pageof 185