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Ophthalmic Genetics|May 5, 2025
Are vitamin D receptor gene rs731236, rs2228570 and NOS3 gene rs3138808 polymorphisms associated with diabetic retinopathy?Emre Taşkın, Mehmet CoşkunOphthalmic Genetics|March 27, 2025
Detailed structural abnormalities associated with a novel VCAN variant in a family with versican vitreoretinopathyAnny Zhong, Alexander Sumaroka, Jonathan C Tsui, et al.Ophthalmic Genetics|May 22, 2025
Bilateral macular colobomata: expanded phenotype of PCARE/C2ORF71Matteo Pederzolli, Andrea Servillo, Riccardo Sacconi, et al.Ophthalmic Genetics|October 21, 2003
Retinopathy of incontinentia pigmenti: a case report with thirteen years follow-upCarolyn A Cates, Samantha S Dandekar, Declan W Flanagan, et al.Ophthalmic Genetics|May 8, 2013
Association of Mn-SOD mutation (c.47T > C) with various POAG clinical indicesKhaled K Abu-Amero, Altaf A Kondkar, Ahmed Mousa, et al.Ophthalmic Genetics|February 21, 2013
TBK1 and flanking genes in human retinaJohn H Fingert, Benjamin W Darbro, Qining Qian, et al.Ophthalmic Genetics|July 10, 2013
Familial exudative vitreoretinopathy caused by a homozygous mutation in TSPAN12 in a cystic fibrosis infantMarco Savarese, Elide Spinelli, Federico Gandolfo, et al.Ophthalmic Genetics|June 27, 2013
Sequencing analysis of the ATOH7 gene in individuals with optic nerve hypoplasiaSing-Hui Lim, Elizabeth St Germain, Khanh-Nhat Tran-Viet, et al.Ophthalmic Genetics|February 1, 2013
Association of single nucleotide polymorphisms in CFH, ARMS2 and HTRA1 genes with risk of age-related macular degeneration in Egyptian patientsRadwa O Abbas, Hassan M E AzzazyOphthalmic Genetics|January 3, 2013
Identification of a novel LCA6 mutation in an Emirati familyMalika FakhratovaPageof 185