1. Compound heterozygous variants in POR gene identified by whole‐exome sequencing in a Chinese pedigree with cytochrome P450 oxidoreductase deficiency. Issue 2 (16th July 2018) Authors: Hao, Chanjuan; Guo, Jun; Guo, Ruolan; Qi, Zhan; Li, Wei; Ni, Xin Journal: Pediatric investigation Issue: Volume 2:Issue 2(2018) Page Start: 90 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Congenital hyperinsulinism in Chinese patients: 5‐yr treatment outcome of 95 clinical cases with genetic analysis of 55 cases. Issue 3 (2nd February 2015) Authors: Gong, Chunxiu; Huang, Shuyue; Su, Chang; Qi, Zhan; Liu, Fang; Wu, Di; Cao, Bingyan; Gu, Yi; Li, Wenjin; Liang, Xuejun; Liu, Min Journal: Pediatric diabetes Issue: Volume 17:Issue 3(2016) Page Start: 227 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Congenital ichthyosiform erythroderma with a novel variant in ABCA12 in a Chinese patient. Issue 1 (17th March 2020) Authors: Yang, Zhou; Qi, Zhan; Xu, Zhe; Li, Wei; Ma, Lin Journal: Pediatric investigation Issue: Volume 4:Issue 1(2020) Page Start: 51 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Correlates of Long-Term Survival of Patients with pN+ Esophageal Squamous Cell Carcinoma after Esophagectomy. (18th February 2021) Authors: He, Ming; Qi, Zhan; Qiu, Rong; Hu, Yuanping; Li, Juan; Li, Yuekao; Wang, Yuxiang Other Names: Franco Pierfrancesco Academic Editor. Journal: Journal of oncology Issue: Volume 2021(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Exome sequencing as the first‐tier test for pediatric respiratory diseases: A single‐center study. Issue 7 (16th May 2021) Authors: Hao, Chanjuan; Guo, Ruolan; Liu, Jun; Hu, Xuyun; Guo, Jun; Yao, Yao; Zhao, Zhipeng; Qi, Zhan; Yin, Jun; Chen, Lanqin; Wang, Hao; Xu, Baoping; Li, Wei Journal: Human mutation Issue: Volume 42:Issue 7(2021) Page Start: 891 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Genetic variants and mutational spectrum of Chinese Hermansky–Pudlak syndrome patients. (17th August 2020) Authors: Liu, Teng; Yuan, Yefeng; Bai, Dayong; Qi, Zhan; Yang, Lin; Zhang, Tianjiao; Yang, Xiumin; Li, Wei; Wei, Aihua Journal: Pigment cell & melanoma research Issue: Volume 34:Number 1(2021) Page Start: 111 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. GW24-e0802 The study of polymer-free paclitaxel-eluting stent in treatment of coronary heart disease. (1st October 2013) Authors: Wei, Geng; Tongle, Zhang; Ying, Yang; Da, Song; Haiyun, Meng; Qianmei, Liu; Qi, Zhan; Peijun, Wang; Xiang, Tian Journal: Heart Issue: Volume 99(2013)Supplement 3 Page Start: A169 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Instability of BLOC‐2 and BLOC‐3 in Chinese patients with Hermansky‐Pudlak syndrome. (22nd November 2018) Authors: Wei, Aihua; Yuan, Yefeng; Qi, Zhan; Liu, Teng; Bai, Dayong; Zhang, Yingzi; Yu, Jiaying; Yang, Lin; Yang, Xiumin; Li, Wei Journal: Pigment cell & melanoma research Issue: Volume 32:Number 3(2019) Page Start: 373 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Large‐scale analysis of Drosophila core promoter function using synthetic promoters. Issue 2 (14th February 2022) Authors: Qi, Zhan; Jung, Christophe; Bandilla, Peter; Ludwig, Claudia; Heron, Mark; Sophie Kiesel, Anja; Museridze, Mariam; Philippou‐Massier, Julia; Nikolov, Miroslav; Renna Max Schnepf, Alessio; Unnerstall, Ulrich; Ceolin, Stefano; Mühlig, Bettina; Gompel, Nicolas; Soeding, Johannes; Gaul, Ulrike Journal: Molecular systems biology Issue: Volume 18:Issue 2(2022) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Mutations in PRRT2 result in paroxysmal dyskinesias with marked variability in clinical expression. Issue 2 (29th December 2011) Authors: Liu, Qing; Qi, Zhan; Wan, Xin-Hua; Li, Jing-Yun; Shi, Lei; Lu, Qiang; Zhou, Xiang-Qin; Qiao, Lei; Wu, Li-Wen; Liu, Xiu-Qin; Yang, Wei; Liu, Ying; Cui, Li-Ying; Zhang, Xue Journal: Journal of medical genetics Issue: Volume 49:Issue 2(2012) Page Start: 79 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗