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A Spontaneous Nonhuman Primate Model of Myopic Foveoschisis |
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| Tzu-Ni Sin, Sangbae Kim, Yumei Li, Jun Wang, Rui Chen, Sook Hyun Chung, Soohyun Kim, M. Isabel Casanova, Sangwan Park, Zeljka Smit-McBride, Ning Sun, Ori Pomerantz, Jeffrey A. Roberts, Bin Guan, Robert B. Hufnagel, Ala Moshiri, Sara M. Thomasy, Paul A. Sieving, Glenn Yiu |
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| Investigative Opthalmology & Visual Science. 2023; 64(1): 18 |
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Identification of Two Novel Variants in the LRP5 Gene that Cause Familial Exudative Vitreoretinopathy |
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| Yuze Wang, Rulian Zhao, Erkuan Dai, Li Peng, Yunqi He, Mu Yang, Shujin Li |
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| Genetic Testing and Molecular Biomarkers. 2022; |
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Foveal hypoplasia and characteristics of optical components in patients with familial exudative vitreoretinopathy and retinopathy of prematurity |
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| Pei-Ying Chen, Eugene Yu-Chuan Kang, Kuan-Jen Chen, Xiao Chun Ling, Yin-Hsi Chang, Nan-Kai Wang, Laura Liu, Yen-Po Chen, Yih-Shiou Hwang, Chi-Chun Lai, Wei-Chi Wu |
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| Scientific Reports. 2022; 12(1) |
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Genotype-phenotype associations in familial exudative vitreoretinopathy: A systematic review and meta-analysis on more than 3200 individuals |
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| Xiaona Wang, Jun Chen, Hui Xiong, Xuhui Yu, Radouil Tzekov |
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| PLOS ONE. 2022; 17(7): e0271326 |
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Hereditary Metabolic Bone Diseases: A Review of Pathogenesis, Diagnosis and Management |
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| Nipith Charoenngam, Aryan Nasr, Arash Shirvani, Michael F. Holick |
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| Genes. 2022; 13(10): 1880 |
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| Mariana A. Flores Pimentel,Irina De la Huerta,Jacque L. Duncan,Anne M. Slavotinek,Anthony T. Moore,Alejandra G. de Alba Campomanes |
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| RETINAL Cases & Brief Reports. 2021; 15(3): 324 |
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The Presence of Wnt Signaling Mutations in Patients With Diabetic Retinopathy |
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| Omar Moinuddin,Prethy Rao,Edward H. Wood,Maxwell S. Stem,Kimberly A. Drenser,Jeremy D. Wolfe |
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| Journal of VitreoRetinal Diseases. 2020; 4(1): 28 |
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Novel FZD4 and LRP5 mutations in a small cohort of patients with familial exudative vitreoretinopathy (FEVR) |
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| William Carrera,Caleb Ng,Caroline Desler,J. Michael Jumper,Anita Agarwal |
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| Ophthalmic Genetics. 2020; : 1 |
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sA novel splice-site mutation in the LRP5 gene causing Familial Exudative Vitreoretinopathy |
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| Shohreh Shafienia,Malihe Mirzaei,Arghavan Kavosi,Majid Yavarian |
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| Gene Reports. 2020; : 100801 |
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Prenatal diagnosis of Norrie disease after whole exome sequencing of an affected proband during an ongoing pregnancy: a case report |
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| Andrey V. Marakhonov,Irina A. Mishina,Vitaly V. Kadyshev,Svetlana A. Repina,Maria F. Shurygina,Olga A. Shchagina,Natalya N. Vasserman,Tatyana A. Vasilyeva,Sergey I. Kutsev,Rena A. Zinchenko |
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| BMC Medical Genetics. 2020; 21(S1) |
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Frizzled 4
regulates ventral blood vessel remodeling in the zebrafish retina |
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| Lucia Caceres,Sergey V. Prykhozhij,Elizabeth Cairns,Harald Gjerde,Nicole M. Duff,Keon Collett,Mike Ngo,Gheyath K. Nasrallah,Christopher R. McMaster,Matthew Litvak,Johane M. Robitaille,Jason N. Berman |
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Familial exudative retinopathy TSPAN12 positive presenting as bilateral retinal stalks: Late structural and functional findings |
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| Giulia M. Amorelli,Marco H. Ji,Lorenzo Orazi,Fernando Molle,Domenico Lepore |
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| American Journal of Ophthalmology Case Reports. 2019; : 100480 |
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Molecular evolutionary and structural analysis of familial exudative vitreoretinopathy associated FZD4 gene |
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| Suman Seemab,Nashaiman Pervaiz,Rabail Zehra,Saneela Anwar,Yiming Bao,Amir Ali Abbasi |
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| BMC Evolutionary Biology. 2019; 19(1) |
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