X. Qin

Hemophilia care in China: review of care for 417 hemophilia patients from 11 treatment centers in Shanxi Province

Z. Duan, Chao Long, Hua Zhao, 2015, Expert review of hematology.

Spectrum of Molecular Defects in 216 Chinese Families With Hemophilia A: Identification of Noninversion Mutation Hot Spots and 42 Novel Mutations

Linhua Yang, Xiue Liu, X. Qin, 2018, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

Comprehensive analysis of phenotypes and genetics in 21 Chinese families with haemophilia B: characterization of five novel mutations

X. Qin, Zhi-ping Guo, Z.P. Guo, 2014, Haemophilia : the official journal of the World Federation of Hemophilia.

[Expressions of Th17 cells and interleukin 17 in patients with primary immune thrombocytopenia and their clinical significance].

Linhua Yang, X. Qin, Li Zhang, 2012, Zhongguo shi yan xue ye xue za zhi.

Molecular mechanism of a novel Ser362Asn mutation causing inherited FX deficiency in a Chinese family

Linhua Yang, Xiue Liu, X. Qin, 2020, International Journal of Hematology.

Molecular Diagnosis of Hemophilia A and Pathogenesis of Novel F8 Variants in Shanxi, China

G. Wang, X. Qin, Sicheng Bian, 2023, Global Medical Genetics.