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Ophthalmic Genetics|May 17, 2017
Co-inheritance of the membrane frizzled-related protein ocular phenotype and glycogen storage disease type IbMaha Mameesh, Anuradha Ganesh, Beena Harikrishna, et al.Ophthalmic Genetics|May 9, 2017
A unique case series of autosomal recessive bestrophinopathy exhibiting multigenerational inheritanceJoshua S Hardin, G Bradley Schaefer, Ahmed B Sallam, et al.Ophthalmic Genetics|April 20, 2018
Pediatric primary calcific band keratopathy with or without glaucoma from biallelic SLC4A4 mutationsArif O Khan, Omar S BasamhOphthalmic Genetics|April 20, 2018
Progressive expansion of the hyperautofluorescent ring in cone-rod dystrophy patientsLuiz H Lima, Claudio Zett, Vinícius Kniggendorf, et al.Ophthalmic Genetics|April 26, 2018
Targeted next-generation sequencing reveals that a compound heterozygous mutation in phosphodiesterase 6a gene leads to retinitis pigmentosa in a Chinese familyShanshan Zhang, Jie Li, Shujin Li, et al.Ophthalmic Genetics|April 5, 2018
A case of exudative vitreoretinopathy and chorioretinal coloboma associated with microcephaly in a female with contiguous Xp11.3-11.4 deletionAnne-Marie Hinds, Elisabeth Rosser, M Ashwin ReddyOphthalmic Genetics|June 15, 2018
22q11.2 microduplication syndrome and juvenile glaucomaFederico Di Matteo, Paolo Bettin, Giulia Ferrari, et al.Ophthalmic Genetics|June 26, 2018
Vitamin A in Stargardt disease-an evidence-based updateCecilie Aalund Federspiel, Mette Bertelsen, Line KesselOphthalmic Genetics|May 29, 2019
Optical Coherence Tomography Angiography (OCT-A) in young choroideremia (CHM) patientsVittoria Murro, Dario Pasquale Mucciolo, Dario Giorgio, et al.Ophthalmic Genetics|March 11, 2022
Inherited retinal dystrophies in a Kuwaiti tribeM G Pandova, T Abduljalil, A E Elshafey, et al.Pageof 185