Xu GQ - Search Results

1

[Analysis of phenotype and genotype in four Chinese pedigrees with inherited coagulation factor V deficiency.].

Huang DD, Wang XF, Chen HY, Xu GQ, Zhang LW, Dai J, Lu YL, Ding QL, Xi XD, Wang HL. Huang DD, et al. Among authors: xu gq. Zhonghua Xue Ye Xue Za Zhi. 2010 Mar;31(3):149-53. Zhonghua Xue Ye Xue Za Zhi. 2010. PMID: 20510101 Chinese.

2

[Studies on inherited coagulation factor VII deficiency and tissue factor abnormality in a pedigree].

Ding QL, Wang XF, Xu GQ, Huang XP, Hu YQ, Wu WM, Fu QH, Wang HL, Wang ZY. Ding QL, et al. Among authors: xu gq. Zhonghua Xue Ye Xue Za Zhi. 2006 Mar;27(3):150-3. Zhonghua Xue Ye Xue Za Zhi. 2006. PMID: 16792912 Chinese.

3

Identification of a novel splicing mutation in the fibrinogen Aalpha chain gene leading to hypofibrinogenaemia in a Chinese pedigree.

Chen H, Wang X, Su X, Yang F, Lu Y, Xu G, Dai J, Ding Q, Xi X, Wang H. Chen H, et al. Haemophilia. 2009 Jan;15(1):394-7. doi: 10.1111/j.1365-2516.2008.01835.x. Epub 2008 Sep 4. Haemophilia. 2009. PMID: 18771425 No abstract available.

4

[The application of thrombin generation tests to warfarin anticoagulation monitoring].

Chen HY, Ding QL, Zhang LW, Xu GQ, Dai J, Wang XF, Xi XD, Wang HL. Chen HY, et al. Among authors: xu gq. Zhonghua Xue Ye Xue Za Zhi. 2008 Mar;29(3):168-70. Zhonghua Xue Ye Xue Za Zhi. 2008. PMID: 18788615 Chinese.

5

[Two new mutations of AT gene in type I inherited antithrombin deficiency.].

Chen Q, Lu YL, Xu GQ, Ding QL, Wang XF, Xi XD, Wang HL. Chen Q, et al. Among authors: xu gq. Zhonghua Xue Ye Xue Za Zhi. 2010 Mar;31(3):145-8. Zhonghua Xue Ye Xue Za Zhi. 2010. PMID: 20510100 Chinese.

6

[Phenotype and genotype analysis of three Chinese pedigrees with von Willebrand disease].

Qin HH, Wang XF, Ding QL, Xu GQ, Zhang LW, Dai J, Lu YL, Xi XD, Wang HL. Qin HH, et al. Among authors: xu gq. Zhonghua Xue Ye Xue Za Zhi. 2011 Feb;32(2):99-102. Zhonghua Xue Ye Xue Za Zhi. 2011. PMID: 21429375 Chinese.

7

[Analysis of phenotype and genotype in three Chinese pedigrees with inherited dysfibrinogenemia].

Ouyang Q, Ding QL, Huang DD, Xu GQ, Zhang LW, Dai J, Lu YL, Wang XF, Xi XD, Wang HL. Ouyang Q, et al. Among authors: xu gq. Zhonghua Xue Ye Xue Za Zhi. 2011 Mar;32(3):153-7. Zhonghua Xue Ye Xue Za Zhi. 2011. PMID: 21535951 Chinese.

8

[Two novel mutations in one pedigree with hereditary Factor VII deficiency].

Xing ZF, Wang XF, Dai J, Lu YL, Xu GQ, Xi XD, Wang HL. Xing ZF, et al. Among authors: xu gq. Zhonghua Xue Ye Xue Za Zhi. 2011 Mar;32(3):158-62. Zhonghua Xue Ye Xue Za Zhi. 2011. PMID: 21535952 Chinese.

9

[Molecular mechanisms of recurrent venous thrombosis in two pedigrees with type I antithrombin deficiency].

Xia Y, Ding QL, Xu GQ, Zhang LW, Dai J, Lu YL, Wang XF, Xi XD, Wang HL. Xia Y, et al. Among authors: xu gq. Zhonghua Xue Ye Xue Za Zhi. 2011 Dec;32(12):848-53. Zhonghua Xue Ye Xue Za Zhi. 2011. PMID: 22339960 Chinese.

10

[Genotype and function analyses of four inherited dysfibrinogenemia pedigree caused by Arg16 amino acid substitution in fibrinogen Aα chain].

Jiang LL, Wang XF, Ding QL, Xu GQ, Zhang LW, Dai J, Lu YL, Xi XD, Wang HL. Jiang LL, et al. Among authors: xu gq. Zhonghua Xue Ye Xue Za Zhi. 2012 Jun;33(6):475-9. Zhonghua Xue Ye Xue Za Zhi. 2012. PMID: 22967385 Chinese.

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