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Ophthalmic Genetics|October 3, 2019
Multimodal retinal imaging of familial amyloid polyneuropathyMarta Latasiewicz, Anna Sala-Puigdollers, Andrea Gonzalez-Ventosa, et al.
Ophthalmic Genetics|October 3, 2019
Modification of the PROM1 disease phenotype by a mutation in ABCA4Winston Lee, Maarjaliis Paavo, Jana Zernant, et al.
Ophthalmic Genetics|July 20, 2019
Estrogen receptor gene polymorphisms and their influence on clinical status of Caucasian patients with primary open angle glaucomaEwa Kosior-Jarecka, Małgorzata Sagan, Dominika Wróbel-Dudzińska, et al.
Ophthalmic Genetics|November 21, 2018
Molecular characterization of Axenfeld-Rieger spectrum and other anterior segment dysgeneses in a sample of Mexican patientsNancy Hernández-Martínez, Ariadna González-Del Angel, Miguel Angel Alcántara-Ortigoza, et al.
Ophthalmic Genetics|February 23, 2021
Multimodal imaging of an RPGR carrier femaleDavid A Kilgore, Tyler A Kilgore, Suporn Sukpraprut-Braaten, et al.
Ophthalmic Genetics|February 8, 2021
Cascade of interactions between candidate genes reveals convergent mechanisms in keratoconus disease pathogenesisAvinash M Veerappa
Ophthalmic Genetics|October 30, 2004
Color vision testingAlex Melamud, Stephanie Hagstrom, Elias Traboulsi
Ophthalmic Genetics|October 30, 2004
Are Duane syndrome and infantile esotropia allelic?Benjamin J Connell, Robin M Wilkinson, Julie M Barbour, et al.
Ophthalmic Genetics|October 21, 2003
Phenotypic variability in three carriers from a family with choroideremia and a frameshift mutation 1388delCCinsG in the REP-1 geneGünther Rudolph, Markus Preising, Petros Kalpadakis, et al.
Ophthalmic Genetics|April 13, 2005
Penetrance and phenotype of the Thr377Met Myocilin mutation in a large Finnish family with juvenile- and adult-onset primary open-angle glaucomaPäivi Puska, Susanna Lemmelä, Paula Kristo, et al.
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