Showing results (341-350 of 1,842) with videos related to
Sort By:
Pageof 185
Ophthalmic Genetics|June 1, 1995
Uveal melanoma and familial atypical mole and melanoma (FAM-M) syndromeA D Singh, C L Shields, J A Shields, et al.Ophthalmic Genetics|June 1, 1995
Multipoint linkage analysis and homogeneity tests in 15 Dutch X-linked retinitis pigmentosa familiesA A Bergen, L I Van den Born, E J Schuurman, et al.Ophthalmic Genetics|June 1, 1995
A complex chromosome translocation resulting in deletion 11p and associated with uveal colobomataR Friling, Y Yassur, D Abeliovich, et al.Ophthalmic Genetics|October 26, 2019
An Ashkenazi Jewish founder mutation in CACNA1F causes retinal phenotype in both hemizygous males and heterozygous female carriersAdva Kimchi, Vardiella Meiner, Shira Silverstein, et al.Ophthalmic Genetics|October 23, 2019
Is ultra wide-field retinal imaging alone appropriate for retinal angioma screening in lower risk subjects attending Von Hippel-Lindau (VHL) clinics?S Mansfield Smith, R Makam, L Sullivan, et al.Ophthalmic Genetics|July 19, 2016
SCARB1 rs5888 is associated with the risk of age-related macular degeneration susceptibility and an impaired macular areaDaiva Stanislovaitiene, Dalia Zaliuniene, Algimantas Krisciukaitis, et al.Ophthalmic Genetics|August 26, 2025
Neuro-ophthalmic complications of endosteal hyperostosis, Worth type: the importance of ophthalmic monitoringAisling Higham, Laura M Watts, Dipesh Rao, et al.Ophthalmic Genetics|May 20, 1998
Summary of ocular genetic disorders and inherited systemic conditions with eye findingsI M MacDonald, P M Haney, M A MusarellaOphthalmic Genetics|May 20, 1998
Prolidase deficiency associated with pathologic myopiaH Kiratli, M SatilmişOphthalmic Genetics|April 16, 2021
Keratoconus in a child with partial trisomy 13Julia Ernst, Amgad Eldib, Hannah L Scanga, et al.Pageof 185