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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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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The application of thrombin generation tests to warfarin anticoagulation monitoring
Chen, Hua-Yun, Ding, Qiu-Lan, Zhang, Li-Wei, Xu, Guan-Qun, Dai, Jing, Wang, Xue-Feng, Xi, Xiao-Dong, Wang, Hong-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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Studies on inherited coagulation factor VII deficiency and tissue factor abnormality in a pedigree
Ding, Qiu-lan, Wang, Xue-feng, Xu, Guan-qun, Huang, Xia-ping, Hu, Yi-qun, Wu, Wen-man, Fu, Qi-hua, Wang, Hong-li, Wang, Zhen-yi
Published in Zhōnghuá xuèyèxué zázhì (01.03.2006)
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Published in Zhōnghuá xuèyèxué zázhì (01.03.2006)
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