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Ophthalmic Genetics|September 3, 2010
(106)Ruthenium brachytherapy for ciliary recurrence with supraciliary effusion in retinoblastomaJay Chhablani, Antonio Romanzo, Aubin Balmer, et al.Ophthalmic Genetics|June 24, 2010
Clinical characterization and proposed mechanism of juvenile glaucoma--a patient with a chromosome 4p deletion, Wolf-Hirschhorn SyndromeJeremy Curtin, Greg Moloney, John Grigg, et al.Ophthalmic Genetics|March 1, 2021
Norrie disease with a spontaneously shrinking choroid plexus abnormality: a case reportSubhi Talal Younes, James Mason Shiflett, Kristin Weaver, et al.Ophthalmic Genetics|March 11, 2021
Congenital stationary night blindness in a patient with mild learning disability due to a compound heterozygous microdeletion of 15q13 and a missense mutation in TRPM1M Delle Fave, M Cordonnier, L Vallee, et al.Ophthalmic Genetics|April 16, 2024
Corneal endothelial cell morphology in children with autosomal recessive Alport syndrome: a longitudinal studyAyna Sariyeva Ismayilov, Okan AkaciOphthalmic Genetics|April 7, 2016
Long-term audiologic follow-up of carboplatin-treated children with retinoblastomaMadelon L Geurtsen, Wijnanda A Kors, Annette C Moll, et al.Ophthalmic Genetics|March 12, 2016
Trabeculectomy in eyes with unsuspected retinoblastomaBhavna Chawla, Maya Hada, Rachna Seth, et al.Ophthalmic Genetics|April 21, 2016
Posterior amorphous corneal dystrophy caused by a de novo deletionS Odent, I Casteels, C Cassiman, et al.Ophthalmic Genetics|April 21, 2016
A novel mutation in ACTG1 causing Baraitser-Winter syndrome with extremely variable expressivity in three generationsAndrew Kemerley, Christina Sloan, Wanda Pfeifer, et al.Ophthalmic Genetics|June 30, 2016
Clinical and genetic characterization of a large primary open angle glaucoma pedigreeMohideen Abdul Kader, Prasanthi Namburi, Sarika Ramugade, et al.Pageof 185