Wang X - Search Results

1

Phenotype and genotype of FXIII deficiency in two unrelated probands: identification of a novel F13A1 large deletion mediated by complex rearrangement.

Ma S, Chen C, Liang Q, Wu X, Wang X, Wu W, Liu Y, Ding Q. Ma S, et al. Among authors: wang x. Orphanet J Rare Dis. 2019 Jul 24;14(1):182. doi: 10.1186/s13023-019-1144-z. Orphanet J Rare Dis. 2019. PMID: 31340840 Free PMC article.

2

[Identification of two novel mutation in two Chinese hereditary coagulation factor XIII deficiency families].

Duan B, Wang H, Chu H, Wang X, Qu B, Li D, Wang H, Yin J, Kang W, Wang Z. Duan B, et al. Among authors: wang h, wang x, wang z. Zhonghua Xue Ye Xue Za Zhi. 2002 Mar;23(3):117-20. Zhonghua Xue Ye Xue Za Zhi. 2002. PMID: 12015062 Chinese.

3

[Molecular analysis of two pedigrees with hereditary F VII deficiency].

Chu H, Wang H, Wang X, Guo X, Qu B, Duan B, Yin J, Kang W, Wang Z. Chu H, et al. Among authors: wang h, wang x, wang z. Zhonghua Xue Ye Xue Za Zhi. 2002 Mar;23(3):130-3. Zhonghua Xue Ye Xue Za Zhi. 2002. PMID: 12015065 Chinese.

4

[Type I antithrombin deficiency due to 13389G deletion in antithrombin gene].

Fu Q, Xu X, Ding Q, Hu Y, Wang X, Wang H. Fu Q, et al. Among authors: wang x, wang h. Zhonghua Xue Ye Xue Za Zhi. 2002 Nov;23(11):588-90. Zhonghua Xue Ye Xue Za Zhi. 2002. PMID: 12482344 Chinese.

5

[In vitro expression of human factor VIII gene induced by sodium butyrate].

Yin J, Wang H, Wang X, Chu H, Li D, Chen H, Fu Q, Duan B, Kang W, Ding Q, Qi Z, Wang Z. Yin J, et al. Among authors: wang h, wang x, wang z. Zhonghua Xue Ye Xue Za Zhi. 2002 Sep;23(9):463-5. Zhonghua Xue Ye Xue Za Zhi. 2002. PMID: 12482356 Chinese.

6

Deficiency of factor XIII gene in Chinese: 3 novel mutations.

Duan B, Wang X, Chu H, Hu Y, Huang X, Qu B, Wang H, Wang Z. Duan B, et al. Among authors: wang x, wang h, wang z. Int J Hematol. 2003 Oct;78(3):251-5. doi: 10.1007/BF02983803. Int J Hematol. 2003. PMID: 14604285

7

[Inherited dysfibrinogenemia caused by Arg275His in the beta chain of fibrinogen].

Fang Y, Wang X, Qi H, Wu W, Ding Q, Dai J, Zhou R, Wang W, Xie S, Wang H. Fang Y, et al. Among authors: wang x, wang h, wang w. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Apr;22(2):201-3. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005. PMID: 15793786 Chinese.

8

Novel aberrant splicings caused by a splice site mutation (IVS1a+5g>a) in F7 gene.

Ding Q, Wu W, Fu Q, Wang X, Hu Y, Wang H, Wang Z. Ding Q, et al. Among authors: wang x, wang h, wang z. Thromb Haemost. 2005 Jun;93(6):1077-81. doi: 10.1160/TH04-04-0220. Thromb Haemost. 2005. PMID: 15968391

9

Gene symbol: F2. Disease: Hypoprothrombinemia.

Wang H, Wang W, Fu Q, Zhou R, Wu W, Ding Q, Hu Y, Wang X, Wang Z. Wang H, et al. Among authors: wang x, wang w, wang z. Hum Genet. 2005 May;116(6):543. Hum Genet. 2005. PMID: 15991329 No abstract available.

10

Recombination in a Chinese haemophilia A family.

Lu Y, Wang X, Ding Q, Dai J, Xi X, Wang H. Lu Y, et al. Among authors: wang x, wang h. Pathology. 2008 Oct;40(6):635-8. doi: 10.1080/00313020802230029. Pathology. 2008. PMID: 18752135 No abstract available.

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