Wang H - Search Results

1

Spectrum of F9 mutations in Chinese haemophilia B patients: identification of 20 novel mutations.

Yu T, Dai J, Liu H, Ding Q, Lu Y, Wang H, Wang X, Fu Q. Yu T, et al. Among authors: wang h, wang x. Pathology. 2012 Jun;44(4):342-7. doi: 10.1097/PAT.0b013e328353443d. Pathology. 2012. PMID: 22544209

2

[Identification of two novel factor XI non-sense mutation Trp228stop and Trp383stop in a Chinese pedigree of congenital factor XI deficiency].

Wu WM, Wang HL, Wang XF, Chu HY, Fu QH, Ding QL, Hu YQ, Shen ZX, Wang ZY. Wu WM, et al. Zhonghua Xue Ye Xue Za Zhi. 2003 Mar;24(3):126-8. Zhonghua Xue Ye Xue Za Zhi. 2003. PMID: 12697122 Chinese.

3

Ser234Leu missense mutation in the A1 domain of factor V causing moderate factor V deficiency in a Chinese family.

Jin PP, Wang XF, Ding QL, Fu QH, Cai XH, Shen LS, Wang HL. Jin PP, et al. Pathology. 2009;41(6):566-71. doi: 10.1080/00313020903072734. Pathology. 2009. PMID: 19900106

4

[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. Zhonghua Xue Ye Xue Za Zhi. 2011 Mar;32(3):158-62. Zhonghua Xue Ye Xue Za Zhi. 2011. PMID: 21535952 Chinese.

5

[Molecular analysis of a patient with hemophilia A caused by FVIII His99Arg mutation].

Qin HH, Wang XF, Ding QL, Lu YL, Dai J, Xi XD, Wang HL. Qin HH, et al. Zhonghua Xue Ye Xue Za Zhi. 2011 Sep;32(9):587-91. Zhonghua Xue Ye Xue Za Zhi. 2011. PMID: 22338150 Chinese.

6

[The molecular mechanism of haemophilia B caused by the Arg327Ile novel mutation in FIX gene in vitro expression].

Zhou JW, Dai J, Ding QL, Yu TT, Lu YL, Wang XF, Wang HL. Zhou JW, et al. Zhonghua Xue Ye Xue Za Zhi. 2012 Aug;33(8):642-7. Zhonghua Xue Ye Xue Za Zhi. 2012. PMID: 23134860 Chinese.

7

Hereditary protein C deficiency caused by compound heterozygous mutants in two independent Chinese families.

Wu YT, Yue F, Wang M, Lu YL, Dai J, Ding QL, Wang HL, Chen HF, Wang XF. Wu YT, et al. Pathology. 2014 Dec;46(7):630-5. doi: 10.1097/PAT.0000000000000165. Pathology. 2014. PMID: 25393254

8

Molecular basis and thrombotic manifestations of antithrombin deficiency in 15 unrelated Chinese patients.

Ding Q, Wang M, Xu G, Ye X, Xi X, Yu T, Wang X, Wang H. Ding Q, et al. Among authors: wang x, wang h, wang m. Thromb Res. 2013 Sep;132(3):367-73. doi: 10.1016/j.thromres.2013.07.013. Epub 2013 Aug 8. Thromb Res. 2013. PMID: 23932013

9

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

Huang D, Chen H, Hu X, Wang X, Wang H. Huang D, et al. Among authors: wang x, wang h. Pathology. 2015 Feb;47(2):145-50. doi: 10.1097/PAT.0000000000000213. Pathology. 2015. PMID: 25551304

10

Clinical features and molecular basis of 102 Chinese patients with congenital dysfibrinogenemia.

Zhou J, Ding Q, Chen Y, Ouyang Q, Jiang L, Dai J, Lu Y, Wu X, Liang Q, Wang H, Wang X. Zhou J, et al. Among authors: wang h, wang x. Blood Cells Mol Dis. 2015 Dec;55(4):308-15. doi: 10.1016/j.bcmd.2015.06.002. Epub 2015 Jun 14. Blood Cells Mol Dis. 2015. PMID: 26460252

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

152,735 results

Search Page

Filters