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	1.	R102W mutation in the RS1 gene responsible for retinoschisis and recurrent glaucoma. [electronic resource] by Huang, Xiu-Feng Tu, Chang-Sen Xing, Dong-Jun Gan, De-Kang Xu, Ge-Zhi Jin, Zi-Bing Producer: 20140317 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)
	2.	Targeted exome sequencing identified novel USH2A mutations in Usher syndrome families. [electronic resource] by Huang, Xiu-Feng Xiang, Ping Chen, Jie Xing, Dong-Jun Huang, Na Min, Qingjie Gu, Feng Tong, Yi Pang, Chi-Pui Qu, Jia Jin, Zi-Bing Producer: 20140110 In: PloS one vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Comprehensive molecular diagnosis of Bardet-Biedl syndrome by high-throughput targeted exome sequencing. [electronic resource] by Xing, Dong-Jun Zhang, Hong-Xing Huang, Na Wu, Kun-Chao Huang, Xiu-Feng Huang, Fang Tong, Yi Pang, Chi-Pui Qu, Jia Jin, Zi-Bing Producer: 20141230 In: PloS one vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Molecular genetic analysis of patients with sporadic and X-linked infantile nystagmus. [electronic resource] by Zhao, Hui Huang, Xiu-Feng Zheng, Zhi-Li Deng, Wen-Li Lei, Xin-Lan Xing, Dong-Jun Ye, Liang Xu, Su-Zhong Chen, Jie Zhang, Fang Yu, Xin-Ping Jin, Zi-Bing Producer: 20170102 In: BMJ open vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)