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	1.	A novel p.R890C mutation in EPHA2 gene associated with progressive childhood posterior cataract in a Chinese family. [electronic resource] by Shentu, Xing-Chao Zhao, Su-Juan Zhang, Li Miao, Qi Producer: 20130301 In: International journal of ophthalmology vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Chinese family with atypical granular corneal dystrophy type I caused by the typical R555W mutation in TGFBI. [electronic resource] by Zhao, Su-Juan Zhu, Ya-Nan Shentu, Xing-Chao Miao, Qi Producer: 20130830 In: International journal of ophthalmology vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Electron microscopic investigation of anterior lens capsule in an individual with true exfoliation. [electronic resource] by Shentu, Xing-Chao Zhu, Ya-Nan Gao, Ying-Hui Zhao, Su-Juan Tang, Ye-Lei Producer: 20130830 In: International journal of ophthalmology vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Oxidation pretreatment by calcium hypochlorite to improve the sensitivity of enzyme inhibition-based detection of organophosphorus pesticides. [electronic resource] by Yang, Xiao Dai, Juan Yang, Li Ma, Ming Zhao, Su-Juan Chen, Xiang-Gui Xiao, Hang Producer: 20180419 In: Journal of the science of food and agriculture vol. 98 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Ocular findings in syndromic gingival fibromatosis: a case study and electronic microscopic investigation of lens. [electronic resource] by Tang, Ye-Lei Shentu, Xing-Chao Zhao, Su-Juan Tang, Xia-Jing He, Long Ping, Fei-Yun Producer: 20140626 In: International journal of ophthalmology vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Novel mutation c.980_983delATTA compound with c.986C>A mutation of the FRMD7 gene in a Chinese family with X-linked idiopathic congenital nystagmus. [electronic resource] by Song, Feng-wei Chen, Bin-bin Sun, Zhao-hui Wu, Li-ping Zhao, Su-juan Miao, Qi Tang, Xia-jing Producer: 20140115 In: Journal of Zhejiang University. Science. B vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Identification of a novel frameshift mutation in PITX2 gene in a Chinese family with Axenfeld-Rieger syndrome. [electronic resource] by Yin, Hou-fa Fang, Xiao-yun Jin, Chong-fei Yin, Jin-fu Li, Jin-yu Zhao, Su-juan Miao, Qi Song, Feng-wei Producer: 20140906 In: Journal of Zhejiang University. Science. B vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)