Hereditary protein C deficiency caused by compound heterozygous mutants in two independent Chinese families
Wu, Ying-Ting, Yue, Fei, Wang, Min, Lu, Ye-Ling, Dai, Jing, Ding, Qiu-Lan, Wang, Hong-Li, Chen, Hui-Fen, Wang, Xue-Feng
Published in Pathology (01.12.2014)
Published in Pathology (01.12.2014)
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Molecular basis of type I antithrombin deficiency in two women with recurrent venous thromboembolism in the first trimester of pregnancy
Xia, Yan, Lu, Qiu-Ya, Lu, Ye-Ling, Dai, Jing, Ding, Qiu-Lan, Wang, Xue-Feng, Xi, Xiao-Dong, Wang, Hong-Li
Published in Blood cells, molecules, & diseases (15.04.2012)
Published in Blood cells, molecules, & diseases (15.04.2012)
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The binding mechanisms of F VIII Trp1707Ser mutation-associated inhibitor
Wu, Xi, Lu, Ye-ling, Ding, Qiu-lan, Dai, Jing, Xi, Xiao-dong, Wang, Hong-li, Wang, Xue-feng
Published in Zhōnghuá xuèyèxué zázhì (01.08.2013)
Published in Zhōnghuá xuèyèxué zázhì (01.08.2013)
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Functional study of abnormal fibrinogen caused by Arg275His mutation in fibrinogen γ chain
Zhou, Jing-yi, Wang, Xue-feng, Ding, Qiu-lan, Xu, Guan-qun, Zhang, Li-wei, Dai, Jing, Lu, Ye-ling, Xi, Xiao-dong, Wang, Hong-li
Published in Zhōnghuá xuèyèxué zázhì (01.03.2013)
Published in Zhōnghuá xuèyèxué zázhì (01.03.2013)
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Phenotype and genotype analysis of two Chinese pedigrees with type 3 von Willebrand diseases
Jiang, Lin-lin, Wang, Xue-feng, Ding, Qiu-lan, Xu, Guan-qun, Zhang, Li-wei, Dai, Jing, Lu, Ye-ling, Wang, Hong-li, Xi, Xiao-dong
Published in Zhonghua yi xue yi chuan xue za zhi (01.10.2012)
Published in Zhonghua yi xue yi chuan xue za zhi (01.10.2012)
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The phenotypic and genotypic diagnosis of three Chinese patients with von Willebrand disease
Jiang, Lin-lin, Cao, Ya-nan, Wang, Xue-feng, Ding, Qiu-lan, Xu, Guan-qun, Zhang, Li-wei, Dai, Jing, Lu, Ye-ling, Wang, Hong-li, Xi, Xiao-dong
Published in Chung-hua nei kʿo tsa chih (01.10.2012)
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Published in Chung-hua nei kʿo tsa chih (01.10.2012)
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Molecular analysis of a patient with hemophilia A caused by FVIII His99Arg mutation
Qin, Huan-huan, Wang, Xue-feng, Ding, Qiu-lan, Lu, Ye-ling, Dai, Jing, Xi, Xiao-dong, Wang, Hong-li
Published in Zhōnghuá xuèyèxué zázhì (01.09.2011)
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Published in Zhōnghuá xuèyèxué zázhì (01.09.2011)
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Genotype and function analyses of four inherited dysfibrinogenemia pedigree caused by Arg16 amino acid substitution in fibrinogen Aα chain
Jiang, Lin-lin, Wang, Xue-feng, Ding, Qiu-lan, Xu, Guan-qun, Zhang, Li-wei, Dai, Jing, Lu, Ye-ling, Xi, Xiao-dong, Wang, Hong-li
Published in Zhōnghuá xuèyèxué zázhì (01.06.2012)
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Published in Zhōnghuá xuèyèxué zázhì (01.06.2012)
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Two novel mutations in one pedigree with hereditary Factor VII deficiency
Xing, Zhi-fang, Wang, Xue-feng, Dai, Jing, Lu, Ye-ling, Xu, Guan-qun, Xi, Xiao-dong, Wang, Hong-li
Published in Zhōnghuá xuèyèxué zázhì (01.03.2011)
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Published in Zhōnghuá xuèyèxué zázhì (01.03.2011)
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Molecular mechanisms of recurrent venous thrombosis in two pedigrees with type I antithrombin deficiency
Xia, Yan, Ding, Qiu-lan, Xu, Guan-qun, Zhang, Li-wei, Dai, Jing, Lu, Ye-ling, Wang, Xue-feng, Xi, Xiao-dong, Wang, Hong-li
Published in Zhōnghuá xuèyèxué zázhì (01.12.2011)
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Published in Zhōnghuá xuèyèxué zázhì (01.12.2011)
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Analysis of phenotype and genotype in three Chinese pedigrees with inherited dysfibrinogenemia
Ouyang, Qi, Ding, Qiu-lan, Huang, Dan-dan, Xu, Guan-qun, Zhang, Li-wei, Dai, Jing, Lu, Ye-ling, Wang, Xue-feng, Xi, Xiao-dong, Wang, Hong-li
Published in Zhōnghuá xuèyèxué zázhì (01.03.2011)
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Published in Zhōnghuá xuèyèxué zázhì (01.03.2011)
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Analysis of phenotype and genotype in four Chinese pedigrees with inherited coagulation factor V deficiency.
Huang, Dan-Dan, Wang, Xue-Feng, Chen, Hua-Yun, Xu, Guan-Qun, Zhang, Li-Wei, Dai, Jin, Lu, Ye-Ling, Ding, Qiu-Lan, Xi, Xiao-Dong, Wang, Hong-Li
Published in Zhōnghuá xuèyèxué zázhì (01.03.2010)
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Published in Zhōnghuá xuèyèxué zázhì (01.03.2010)
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Phenotype and genotype analysis of three Chinese pedigrees with von Willebrand disease
Qin, Huan-huan, Wang, Xue-feng, Ding, Qiu-lan, Xu, Guan-qun, Zhang, Li-wei, Dai, Jing, Lu, Ye-ling, Xi, Xiao-dong, Wang, Hong-li
Published in Zhōnghuá xuèyèxué zázhì (01.02.2011)
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Published in Zhōnghuá xuèyèxué zázhì (01.02.2011)
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Two new mutations of AT gene in type I inherited antithrombin deficiency.
Chen, Qiong, Lu, Ye-Ling, Xu, Guan-Qun, Ding, Qiu-Lan, Wang, Xue-Feng, Xi, Xiao-Dong, Wang, Hong-Li
Published in Zhōnghuá xuèyèxué zázhì (01.03.2010)
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Published in Zhōnghuá xuèyèxué zázhì (01.03.2010)
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Detection of factor IX gene mutation in patients with hemophilia B by DNA sequencing
Zhang, Yuan, Yang, Lin-Hua, Lu, Ye-Ling, Ding, Qiu-Lan, Wang, Xue-Feng, Liu, Xiu-E, Hou, Li-Hong
Published in Zhongguo shi yan xue ye xue za zhi (01.04.2009)
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Published in Zhongguo shi yan xue ye xue za zhi (01.04.2009)
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Gene diagnosis of 3 haemophilia B families
Zhang, Yuan, Yang, Lin-Hua, Lu, Ye-Ling, Ding, Qiu-Lan, Wang, Xue-Feng, Liu, Xiu-E, Zhang, Li
Published in Zhōnghuá xuèyèxué zázhì (01.03.2008)
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Published in Zhōnghuá xuèyèxué zázhì (01.03.2008)
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