41. A novel gene insertion combined with a missense mutation causing factor VII deficiency in two unrelated Chinese families. Issue 6 (September 2015) Authors: Hao, Xiuping; Cheng, XiaoLi; Wang, Yingyu; Yang, LiHong; Xie, Yaosheng; Wang, Mingshan; Jin, Yanhui Journal: Blood coagulation and fibrinolysis Issue: Volume 26:Issue 6(2015) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
42. A novel heterozygous mutation (γIIe367Thr) causes congenital dysfibrinogenemia in a Chinese family. Issue 8 (December 2020) Authors: Luo, Shasha; Xu, Qiyu; Xie, Yaosheng; Li, Xiaolong; Jin, Yanhui; Yang, Lihong; Liu, Siqi; Wang, Mingshan Journal: Blood coagulation and fibrinolysis Issue: Volume 31:Issue 8(2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
43. A novel heterozygous mutation flanking the fourth calcium-binding domain of the ITGA2B gene induces severe bleeding complications: a case report and literature review. Issue 2 (2nd March 2021) Authors: Xu, Qian; Zhou, Min; Xu, Ming; Zhang, Lu; Zhang, Xian Journal: Blood coagulation and fibrinolysis Issue: Volume 32:Issue 2(2021) Page Start: 146 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
44. A novel homozygous mutation (Gly1715Ser) causing hereditary factor V deficiency in a Chinese patient. Issue 1 (January 2020) Authors: Liu, Siqi; Luo, Shasha; Yang, Lihong; Jin, Yanhui; Xie, Haixiao; Xie, Yaosheng; Li, Xiaolong; Wang, Mingshan Journal: Blood coagulation and fibrinolysis Issue: Volume 31:Issue 1(2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
45. A novel missense mutation in F9 gene causes hemophilia B in a family with clinical variability. Issue 2 (March 2020) Authors: Yi, Sheng; Yang, Qi; Zuo, Yangjin; Li, Mengting; Luo, Jingsi; Qin, Zailong; Zhang, Qinle; Li, Meng; Huang, Limei; Lu, Yingchi; Feng, Shihan; Fan, Xin Journal: Blood coagulation and fibrinolysis Issue: Volume 31:Issue 2(2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
46. A novel mutation (Leu60Pro) in a Chinese pedigree with hereditary factor XI deficiency. Issue 6 (September 2021) Authors: Xie, Haixiao; Liu, Meina; Zou, Anqing; Xie, Yaosheng; Ye, Jiajia Journal: Blood coagulation and fibrinolysis Issue: Volume 32:Issue 6(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
47. A novel mutation (Ser951LeufsTer8) in F5 gene leads to hereditary coagulation factor V deficiency. Issue 2 (12th March 2021) Authors: Su, Kankan; Wang, Lin; Wang, Mingshan; Wang, Hong Journal: Blood coagulation and fibrinolysis Issue: Volume 32:Issue 2(2021) Page Start: 140 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
48. A novel mutation (Tyr503Cys) in a severe factor XI deficiency. Issue 3 (April 2018) Authors: Su, Kankan; Cai, Xiaoxiao; Xia, Wenli; Jin, Yanhui; Yang, Lihong; Wang, Mingshan Journal: Blood coagulation and fibrinolysis Issue: Volume 29:Issue 3(2018) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
49. A novel mutation in GP1BA gene leads to mono-allelic Bernard Soulier syndrome form of macrothrombocytopenia. Issue 1 (January 2017) Authors: Ali, Shahnaz; Shetty, Shrimati; Ghosh, Kanjaksha Journal: Blood coagulation and fibrinolysis Issue: Volume 28:Issue 1(2017) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
50. A novel mutation in the GP1BA gene in Bernard–Soulier syndrome. Issue 1 (January 2020) Authors: Özdemir, Zeynep C.; Düzenli Kar, Yeter; Ceylaner, Serdar; Bör, Özcan Journal: Blood coagulation and fibrinolysis Issue: Volume 31:Issue 1(2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗