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Ophthalmic Genetics|November 29, 2016
Vitamin A deficiency due to bi-allelic mutation of RBP4: There's more to it than meets the eyeKamron N Khan, Keren Carss, F Lucy Raymond, et al.Ophthalmic Genetics|December 1, 2016
A decade of age-related macular degeneration risk models: What have we learned from them and where are we going?Michael Zhang, Paul N BairdOphthalmic Genetics|January 26, 2017
Macular hole in Stargardt disease: Clinical and ultra-structural observationStanislao Rizzo, Dario Pasquale Mucciolo, Daniela Bacherini, et al.Ophthalmic Genetics|February 8, 2014
A Study of VEGF Gene Polymorphism in Egyptian Patients with Diabetic RetinopathyRasha Mohamad Hosny Shahin, Mohamad Amr Salah Eddin Abdelhakim, Mohammed El Sayed Mahmoud Owid, et al.Ophthalmic Genetics|March 26, 2008
Asymptomatic renal cell carcinoma as a finding of Bardet Biedl syndromeRenzo A Zaldivar, Matthew D Neale, William E Evans, et al.Ophthalmic Genetics|March 26, 2008
Mutation in the SLC4A11 gene associated with autosomal recessive congenital hereditary endothelial dystrophy in a large Saudi familyShaival S Shah, Ali Al-Rajhi, James D Brandt, et al.Ophthalmic Genetics|February 22, 2014
Hereditary Benign Intraepithelial Dyskeratosis: Report of a Case and Re-examination of the Evidence for Locus HeterogeneityTina Bui, Jonathan W Young, Ricardo F Frausto, et al.Ophthalmic Genetics|February 22, 2014
Clinical and Electrophysiologic Characteristics of a Large Kindred with X-Linked Retinitis Pigmentosa Associated with the RPGR LocusJonathan H Tzu, Tania Arguello, Audina M Berrocal, et al.Ophthalmic Genetics|February 22, 2014
Genotype-phenotype correlations, and retinal function and structure in von Hippel-Lindau diseaseElisabeth Wittström, Margareta Nordling, Sten AndréassonOphthalmic Genetics|February 20, 2014
Advantage of Whole Exome Sequencing over Allele-Specific and Targeted Segment Sequencing in Detection of Novel TULP1 Mutation in Leber Congenital AmaurosisYiran Guo, Ivan Prokudin, Cong Yu, et al.Pageof 185