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Ophthalmic Genetics|December 5, 2022
Fleck-like lesions in CEP290-associated leber congenital amaurosis: a case seriesTomas S Aleman, Erin C O'Neil, Katherine E Uyhazi, et al.
Ophthalmic Genetics|June 29, 2022
Infantile esotropia in a family with TUBB3 mutation associated congenital fibrosis of extraocular musclesYeonji Jang, Eunseo Kwak, Joon-Yong An, et al.
Ophthalmic Genetics|July 7, 2022
Experiences of genetic testing among individuals with retinitis pigmentosaEmily Krauss, Jared Macher, Jenina Capasso, et al.
Ophthalmic Genetics|November 28, 2022
Effects of duration and number of symptoms on vision-related anxiety in patients with Inherited Retinal DiseasesLilia T Popova, Rebhi O Abuzaitoun, Maria Fernanda Abalem, et al.
Ophthalmic Genetics|April 12, 2022
Novel RB1 germline mutation in a healthy manEugenia M Ramos-Dávila, Lucas A Garza-Garza, Rocío Villafuerte-de la Cruz, et al.
Ophthalmic Genetics|April 29, 2022
RP1-associated recessive retinitis pigmentosa caused by paternal uniparental disomyEmma C Bedoukian, Erin C O'Neil, Tomas S Aleman
Ophthalmic Genetics|July 2, 2010
PITPNM3 is an uncommon cause of cone and cone-rod dystrophiesLinda Köhn, Susanne Kohl, Sara J Bowne, et al.
Ophthalmic Genetics|November 12, 2010
Screening genes of the visual cycle RGR, RBP1 and RBP3 identifies rare sequence variationsMohamed Ksantini, Audrey Sénéchal, Béatrice Bocquet, et al.
Ophthalmic Genetics|November 12, 2010
Astrocytic hamartoma of the optic disc and multiple café-au-lait macules in a child with neurofibromatosis type 2Reecha Sachdeva, David A Rothner, Elias I Traboulsi, et al.
Ophthalmic Genetics|November 12, 2010
Hereditary primary lateral sclerosis with cone dysfunctionSri Gore, Lucinda Carr, Anthony Moore, et al.
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