1. Esophageal Carcinosarcoma: Analysis of Clinical Features and Prognosis of 24 Cases and a Literature Review. (13th May 2021) Authors: Chen, Shusen; Shi, Yu; Lu, Zhengjing; Wang, Mingwei; Cong, Longfei; Yang, Baixia; Chen, Xudong; Cai, Jing; Yang, Xi Journal: Cancer control Issue: Volume 28(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Identification of one novel pathogenic ITGB3 mutation and two known mutations in two Chinese pedigrees with hereditary Glanzmann thrombasthenia. (2nd April 2020) Authors: Lu, Zhengjing; Nikuze, Lauriane; Zhong, Zhoulin; Li, Fang; Zhang, Fuyong; Liang, Kairong; Wei, Manlv; Wei, Hongying Journal: Platelets Issue: Volume 31:Number 3(2020) Page Start: 355 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Identification of two novel mutations in three children with congenital factor VII deficiency. Issue 5 (July 2021) Authors: Liang, Kairong; Nikuze, Lauriane; Zhang, Fuyong; Lu, Zhengjing; Wei, Manlv; Wei, Hongying Journal: Blood coagulation and fibrinolysis Issue: Volume 32:Issue 5(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. The novel mutation p.Asp315Tyr causes severe hemophilia B by impairing coagulation factor IX expression. Issue 198 (February 2021) Authors: Lu, Zhengjing; Zhang, Huayang; Chen, Changming; Wu, Wenman; Wei, Hongying Journal: Thrombosis research Issue: Issue 198(2021) Page Start: 23 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗