Evaluation of common COL2A1 gene variants in Iranian patients suspected with Stickler syndrome type I by Fatemeh Abolhasani, Hossein Abdali, Mohammad Kazemi, Bijan Movahedian Attar, Fatemeh Derakhshandeh, Majid Hosseinzadeh

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Genetic and clinical profile of high myopia patients with rhegmatogenous retinal detachment by Lin Zhou, Farrukhjon Boboev, Hui Chen, Fanwen Jiang, Chun Zhang, Jing Xiao, Hui Jiang, Yongchuan Liao, Zhuping Xu

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Diagnosis of congenital ectopia lentis: a case report and review of the literature by Xuebi Cai, Wei Chen, Jiezheng Xue, Junliang Wang, Zhisha Bai, Wei Qiang, Sifang Zhang, Heding Zhou

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Reliability of clinical impressions and optimal genetic diagnostic strategies of heritable connective tissue disorders with ocular involvement in a large Chinese cohort by Qin-Meng Shu, Yu-Qiao Ju, Yuan Zong, Ting Zhang, Xin Huang, Feng-juan Gao, Qing Chang

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Stickler Sendromuna Genel Bakış: Bir Derleme Çalışması by Ayşe Işıldar

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Novel pathogenic splicing mutation in COL11A1 in a patient with Stickler syndrome verified by minigene splicing assay by Jie Zhang, Jie Zhang, Jie Zhang, Yaxin Huang, Yaxin Huang, Yaxin Huang, Yafei Deng, Yafei Deng, Yafei Deng, Xiaochun Yang, Hong Shi, Yuecheng Yang, Tao Lv, Tao Lv, Tao Lv, Yuanlong Yan, Yuanlong Yan, Yuanlong Yan, Ming He, Fang Liu, Fang Liu, Fang Liu

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The frequency of intraocular hemorrhage in hereditary vitreoretinal dystrophies by O. Yu. Yatsenko, O. S. Velibekova

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