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Ophthalmic Genetics|February 18, 2021
An unusual ophthalmic presentation of Wolf-Hirschhorn syndromeGökhan Çelik, Bilge Batu Oto, Osman Kızılay, et al.
Ophthalmic Genetics|February 22, 2021
Genotype-phenotype associations in Danish patients with ocular and oculocutaneous albinismLine Kessel, Birgit Kjer, Ulrikke Lei, et al.
Ophthalmic Genetics|November 24, 2018
Electrophysiological verification of enhanced S-cone syndrome caused by a novel c.755T>C NR2E3 missense variantJasmina Cehajic-Kapetanovic, Charles L Cottriall, Jasleen K Jolly, et al.
Ophthalmic Genetics|August 14, 2019
Clinical and genetic characteristics of nevus of Ota with choroidal melanoma in ChineseXue Pan, Shufeng Zheng
Ophthalmic Genetics|August 17, 2019
Association study of high-frequency variants of MTHFR gene with retinal vein occlusion in a Spanish populationBeatriz Fernández-Vega, Lydia Álvarez, Montserrat García, et al.
Ophthalmic Genetics|August 20, 2019
Choroidal neovascularization in an adolescent with RDH12-associated retinal degenerationShawn Philip, Xiaoyu Xu, Ketan G Laud, et al.
Ophthalmic Genetics|November 17, 2018
Role of the tissue-type plasminogen activator -7351C > T and plasminogen activator inhibitor 1 4G/5G gene polymorphisms in central serous chorioretinopathyEva Maria Malle, Laura Posch-Pertl, Wilfried Renner, et al.
Ophthalmic Genetics|September 10, 2019
Efficacy of topical brinzolamide in children with retinal dystrophiesBrittni A Scruggs, Constance V Chen, Wanda Pfeifer, et al.
Ophthalmic Genetics|February 1, 2017
Leber hereditary optic neuropathy due to a new ND1 mutationPatrick Soldath, Marianne Wegener, Birgit Sander, et al.
Ophthalmic Genetics|February 1, 2017
Cystoid macular changes on optical coherence tomography in a patient with maternally inherited diabetes and deafness (MIDD)-associated macular dystrophyCynthia X Qian, Kari Branham, Naheed Khan, et al.
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