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Ophthalmic Genetics|January 18, 2022
The first reported case of CDH3-related hypotrichosis with juvenile macular dystrophy from Jordan: a case reportKhalid Al Zubi, Nesrin Mwafi, Hamzeh Mohammad Alrawashdeh, et al.Ophthalmic Genetics|February 18, 2021
Retinal dystrophy as part of TTC21B-associated ciliopathyTamar Ben-Yosef, Nurit Asia Batsir, Tahleel Ali Nasser, et al.Ophthalmic Genetics|February 16, 2019
Ophthalmologic findings in the Cornelia de Lange syndromeAngell Shi, Alex V LevinOphthalmic Genetics|September 24, 2019
Near-infrared autofluorescence in young choroideremia patientsDario Pasquale Mucciolo, Vittoria Murro, Dario Giorgio, et al.Ophthalmic Genetics|September 27, 2019
Retinal dystrophy associated with a Kizuna (KIZ) mutation and a predominantly macular phenotypeYue Zhao, Razek Georges Coussa, Meghan J M DeBenedictis, et al.Ophthalmic Genetics|February 25, 2021
Multimodal imaging and genetic findings in a case of ARSG-related atypical Usher syndromeNicholas H Fowler, May I El-Rashedy, Emad A Chishti, et al.Ophthalmic Genetics|April 11, 2017
ADAMTSL4 assessment in ectopia lentis reveals a recurrent founder mutation in PolynesiansKatherine A van Bysterveldt, Rasha Al Taie, Will Ikink, et al.Ophthalmic Genetics|August 9, 2019
Targeted panel sequencing identifies a novel NR2F1 mutations in a patient with Bosch-Boonstra-Schaaf optic atrophy syndromeSung Eun Park, Jihei Sara Lee, Seung-Tae Lee, et al.Ophthalmic Genetics|October 5, 2019
Dilated and tortuous retinal vessels as a sign of Cantu syndromeEli Kisilevsky, Radha P Kohly, Edward A MargolinOphthalmic Genetics|February 23, 2021
Association study of fibroblast growth factor 10 (FGF10) rs399501 polymorphism with susceptibility to high myopia in a Chinese populationXiu Jiang, Tian Tong, Ning Xia, et al.Pageof 185