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Ophthalmic Genetics|January 30, 2023
Investigation of germline VHL variants in Iranian patients with retinal capillary hemangioblastoma and genotype-phenotype analysisMasood Naseripour, Fatemeh Azimi, Said Talebi, et al.
Ophthalmic Genetics|December 5, 2025
The timing of genetic testing and healthcare costs associated with the diagnostic journey of inherited retinal diseaseQiaoyi Zhang, Kirsten Lum, Qian Cai, et al.
Ophthalmic Genetics|August 9, 2012
Craniosynostosis with ectopia lentis and a homozygous 20-base deletion in ADAMTSL4Aman Chandra, Jose Antonio Aragon-Martin, Saba Sharif, et al.
Ophthalmic Genetics|November 10, 2012
Novel susceptibility genes associated with diabetic cataract in a Taiwanese populationHui-Ju Lin, Yu-Chuen Huang, Jane-Ming Lin, et al.
Ophthalmic Genetics|September 7, 2012
Human RNA integrity after postmortem retinal tissue recoveryLuisa Montanini, Stefano Ferrari, Pellegrino Crafa, et al.
Ophthalmic Genetics|October 9, 2012
Peculiar fundus abnormalities and pathognomonic electrophysiological findings in a 14-month-old boy with NR2E3 mutationsCatherine Cassiman, Werner Spileers, Elfride De Baere, et al.
Ophthalmic Genetics|January 15, 2014
Analyses of Sequence Variants in the MYOC Gene and of Single Nucleotide Polymorphisms in the NR3C1 and FKBP5 Genes in Corticosteroid-Induced Ocular HypertensionBarend F Hogewind, Shazia Micheal, Frederieke E Schoenmaker-Koller, et al.
Ophthalmic Genetics|June 10, 2014
Molecular Karyotyping of a Dysmorphic Girl from Saudi Arabia with CYP1B1-negative Primary Congenital GlaucomaKhaled K Abu-Amero, Altaf A Kondkar, Arif O Khan
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