1. A point mutation in Fgf9 impedes joint interzone formation leading to multiple synostoses syndrome. (7th February 2017) Authors: Tang, Lingyun; Wu, Xiaolin; Zhang, Hongxin; Lu, Shunyuan; Wu, Min; Shen, Chunling; Chen, Xuejiao; Wang, Yicheng; Wang, Weigang; Shen, Yan; Gu, Mingmin; Ding, Xiaoyi; Jin, Xiaolong; Fei, Jian; Wang, Zhugang Journal: Human molecular genetics Issue: Volume 26:Number 7(2017:Apr. 01) Page Start: 1280 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. DHTKD1 is essential for mitochondrial biogenesis and function maintenance. Issue 21 (27th September 2013) Authors: Xu, Wangyang; Zhu, Houbao; Gu, Mingmin; Luo, Qingqiong; Ding, Jieying; Yao, Yuting; Chen, Fuxiang; Wang, Zhugang Journal: FEBS letters Issue: Volume 587:Issue 21(2013) Page Start: 3587 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Multimodal imaging and genetic characteristics of Chinese patients with USH2A‐associated nonsyndromic retinitis pigmentosa. Issue 11 (6th September 2020) Authors: Chen, Chong; Sun, Qiao; Gu, Mingmin; Qian, Tianwei; Luo, Dawei; Liu, Kun; Xu, Xun; Yu, Suqin Journal: Molecular genetics & genomic medicine Issue: Volume 8:Issue 11(2020) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Multimodal imaging and genetic characteristics of Chinese patients with USH2A‐associated nonsyndromic retinitis pigmentosa. Issue 11 (6th September 2020) Authors: Chen, Chong; Sun, Qiao; Gu, Mingmin; Qian, Tianwei; Luo, Dawei; Liu, Kun; Xu, Xun; Yu, Suqin Journal: Molecular genetics & genomic medicine Issue: Volume 8:Issue 11(2020) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗