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Ophthalmic Genetics|June 22, 2017
Metallothionein polymorphisms in a Northern Spanish population with neovascular and dry forms of age-related macular degenerationMontserrat García, Lydia Álvarez, Ángela Fernández, et al.
Ophthalmic Genetics|June 22, 2017
Multimodal imaging in CABP4-related retinopathyPatrik Schatz, Maram E A Abdalla Elsayed, Arif O Khan
Ophthalmic Genetics|February 2, 2022
Anophthalmia and microphthalmia in children: associated ocular, somatic and genetic morbidities and quality of lifeCecilia Fahnehjelm, Eva Dafgård Kopp, Josephine Wincent, et al.
Ophthalmic Genetics|October 6, 2021
Ophthalmic manifestations in Costello syndrome caused by Ras pathway dysregulation during developmentSuma P Shankar, Reshmitha Fallurin, Tonya Watson, et al.
Ophthalmic Genetics|July 18, 2022
Retinoblastoma and uveal melanoma in Jordan: incidence, demographics, and survival (2011-2020)Yacoub A Yousef, Mona Mohammad, Ibrahim Al-Nawaiseh, et al.
Ophthalmic Genetics|April 27, 2022
Genetic screening of TGFBI in Iranian patients with TGFBI-associated corneal dystrophies and a meta-analysis of global variation frequenciesRoxanne Jozaei, Mohammad-Ali Javadi, Iman Safari, et al.
Ophthalmic Genetics|December 13, 2023
Foveal hypoplasia in a Chinese adolescent with 48, XXYY syndromeChunli Chen, Sitong Guo, Zhiqin Huang, et al.
Ophthalmic Genetics|November 24, 2023
Band-shaped keratopathy in HNF4A-related Fanconi syndrome: a case report and review of the literatureAnshuman Verma, Dilip Kumar Mishra, Deepak P Edward, et al.
Ophthalmic Genetics|November 6, 2023
An overview of RB1 transcript alterations detected during retinoblastoma genetic screeningElizabeth A Price, Mandeep S Sagoo, M Ashwin Reddy, et al.
Ophthalmic Genetics|September 6, 2023
Neuropathy, ataxia, retinitis pigmentosa: a case of a mother and two siblingsMark Rabinovich, Olivia Zambrowski, Alexandra Miere, et al.
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