X. Wang

The prevalence of factor VIII inhibitors and genetic aspects of inhibitor development in Chinese patients with haemophilia A

Y. Zhao, J. Sun, R. Yang, 2010, Haemophilia : the official journal of the World Federation of Hemophilia.

Risk factors associated with inhibitor development in Chinese patients with haemophilia B

X. Wang, Q. Ding, L. Lin, 2015, Haemophilia : the official journal of the World Federation of Hemophilia.

[Carrier detection and prenatal diagnosis for hemophilia A].

Hong Wang, X. Wang, Y. Liu, 2001, Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi.

Characterization of large deletions in the F8 gene using multiple competitive amplification and the genome walking technique

X. Xi, X. Wang, Q. Ding, 2013, Journal of thrombosis and haemostasis : JTH.

Similarity in joint and mucous bleeding syndromes in type 2N von Willebrand disease and severe hemophilia A coexisting with type 1 von Willebrand disease in two Chinese pedigrees.

X. Xi, X. Wang, Q. Ding, 2014, Blood cells, molecules & diseases.

Characterisation and validation of a novel panel of the six short tandem repeats for genetic counselling in Chinese haemophilia A pedigrees

X. Xi, X. Wang, Q. Ding, 2012, Haemophilia : the official journal of the World Federation of Hemophilia.

Prevalence of the factor 8 gene intron 1 inversion in Chinese haemophiliacs and its application to carrier detection and prenatal diagnosis in haemophilia A families

X. Xi, X. Wang, Q. Ding, 2011, Haemophilia : the official journal of the World Federation of Hemophilia.

Molecular defects in the factor X gene caused by novel heterozygous mutations IVS5+1G>A and Asp409del

X. Xi, X. Wang, Q. Ding, 2013, Haemophilia : the official journal of the World Federation of Hemophilia.