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Ophthalmic Genetics|November 3, 2022
Visual outcome, ocular findings, and visual quality of life in patients with Fabry diseaseMattias Nilsson, Hani Tavakoli Kolagari, David Epstein, et al.Ophthalmic Genetics|November 3, 2022
A typical anterior retinoblastoma: diagnosis by aqueous humor cell-free DNA analysisStephanie N Kletke, Sameh Soliman, Hilary Racher, et al.Ophthalmic Genetics|October 14, 2022
Understanding the propensity to undergo genetic testing in patients affected by inherited retinal diseases: a twelve-item questionnaireLeonardo Bottazzi, Alessio Antropoli, Lorenzo Bianco, et al.Ophthalmic Genetics|October 28, 2022
Association of osteogenesis imperfecta and glaucoma: case reportOksan AlpoganOphthalmic Genetics|September 13, 2022
Hereditary motor and sensory neuropathy type VIA with optic nerve pallor in two sisters with pathologic myopia: a case series and reviewKevin Babu, Kimberly Seamon, Ann Jewell, et al.Ophthalmic Genetics|September 12, 2022
Seroreactivity against retinal proteins in a case of POC1B gene associated cone dystrophy with normal funduscopic appearance: a systematic approach to diagnosisÖzge Yanık, Figen Batıoğlu, Yavuz Sahin, et al.Ophthalmic Genetics|October 4, 2022
Screening of candidate genes at GLC3B and GLC3C loci in Chinese primary congenital glaucoma patients with targeted next generation sequencingYunsheng Qiao, Tingting Shao, Yuhong Chen, et al.Ophthalmic Genetics|February 21, 2022
Novel biallelic AHR splice site mutation cause isolated foveal hypoplasia in Saudi patient: a case reportBasamat AlMoallem, Essam AlharthiOphthalmic Genetics|April 23, 2019
MFSD8 gene mutations; evidence for phenotypic heterogeneityDavood Zare-Abdollahi, Ata Bushehri, Afagh Alavi, et al.Ophthalmic Genetics|August 22, 2018
Retinal detachment and infantile-onset glaucoma in Stickler syndrome associated with known and novel COL2A1 mutationsThomas J Wubben, Kari H Branham, Cagri G Besirli, et al.Pageof 185