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Novel mutation in OCRL leading to a severe form of Lowe syndrome.
Zhou FQ, Wang QW, Liu ZZ, Zhang XL, Wang DN, Dongye MM, Lin HT, Chen WR. Zhou FQ, et al. Among authors: dongye mm. Int J Ophthalmol. 2019 Jul 18;12(7):1057-1060. doi: 10.18240/ijo.2019.07.01. eCollection 2019. Int J Ophthalmol. 2019. PMID: 31341792 Free PMC article.
Loss-of-function mutations in FREM2 disrupt eye morphogenesis.
Zhang X, Wang D, Dongye M, Zhu Y, Chen C, Wang R, Long E, Liu Z, Wu X, Lin D, Chen J, Lin Z, Wang J, Li W, Li Y, Li D, Lin H. Zhang X, et al. Exp Eye Res. 2019 Apr;181:302-312. doi: 10.1016/j.exer.2019.02.013. Epub 2019 Feb 22. Exp Eye Res. 2019. PMID: 30802441
Artificial intelligence manages congenital cataract with individualized prediction and telehealth computing.
Long E, Chen J, Wu X, Liu Z, Wang L, Jiang J, Li W, Zhu Y, Chen C, Lin Z, Li J, Li X, Chen H, Guo C, Zhao L, Nie D, Liu X, Liu X, Dong Z, Yun B, Wei W, Xu F, Lv J, Li M, Ling S, Zhong L, Chen J, Zheng Q, Zhang L, Xiang Y, Tan G, Huang K, Xiang Y, Lin D, Zhang X, Dongye M, Wang D, Chen W, Liu X, Lin H, Liu Y. Long E, et al. NPJ Digit Med. 2020 Aug 28;3:112. doi: 10.1038/s41746-020-00319-x. eCollection 2020. NPJ Digit Med. 2020. PMID: 32904507 Free PMC article.
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[No authors listed] [No authors listed] PMID: 33299079
17 results