Fu Q - Search Results

1

A novel and a previously described compound heterozygous PKLR gene mutations causing pyruvate kinase deficiency in a Chinese child.

Li H, Gu P, Yao RE, Wang J, Fu Q, Wang J. Li H, et al. Among authors: fu q. Fetal Pediatr Pathol. 2014 Jun;33(3):182-90. doi: 10.3109/15513815.2014.890260. Epub 2014 Mar 6. Fetal Pediatr Pathol. 2014. PMID: 24601847

2

[Two novel factor V gene mutations associated with congenital coagulation factor V deficiency, study of one pedigree].

Fu QH, Wang HL, Wang MS, Ding QL, Wu WM, Hu YQ, Wang XF, Wang ZY. Fu QH, et al. Zhonghua Yi Xue Za Zhi. 2003 Feb 25;83(4):312-5. Zhonghua Yi Xue Za Zhi. 2003. PMID: 12812650 Chinese.

3

[Type I hereditary protein C deficiency due to C5498T mutation in protein C gene].

Zhou RF, Wang HL, Fu QH, Wang WB, Wu WM, Ding QL, Xie S, Hu YQ, Wang XF, Wang ZY. Zhou RF, et al. Zhonghua Yi Xue Za Zhi. 2003 Oct 10;83(19):1694-7. Zhonghua Yi Xue Za Zhi. 2003. PMID: 14642106 Chinese.

4

[Double heterozygous mutations of non-canonical splice (IVS1a + 5g > a) and His348Gln caused inherited coagulation factor VII deficiency].

Ding QL, Wang HL, Wang XF, Wang MS, Fu QH, Wu WM, Hu YQ, Wang ZY. Ding QL, et al. Zhonghua Xue Ye Xue Za Zhi. 2004 Mar;25(3):139-42. Zhonghua Xue Ye Xue Za Zhi. 2004. PMID: 15182580 Chinese.

5

[Inherited coagulation factor X deficiency caused by two novel mutations in factor X gene].

Wang WB, Wang HL, Wang XF, Fu QH, Zhou RF, Xie S, Hu YQ, Wang ZY. Wang WB, et al. Zhonghua Xue Ye Xue Za Zhi. 2004 Sep;25(9):519-22. Zhonghua Xue Ye Xue Za Zhi. 2004. PMID: 15569527 Chinese.

6

[Severe hereditary coagulation factor V deficiency caused by two novel heterozygous mutations].

Zhou RF, Fu QH, Xu XC, Wang WB, Wu WM, Ding QL, Xie S, Zhai ZM, Hu YQ, Wang XF, Wu JS, Wang HL. Zhou RF, et al. Zhonghua Xue Ye Xue Za Zhi. 2005 Mar;26(3):129-32. Zhonghua Xue Ye Xue Za Zhi. 2005. PMID: 15946520 Chinese.

7

[A heterozygous point mutation G13328A in antithrombin gene causes thrombosis].

Zhou RF, Shi GC, Fu QH, Wang WB, Xie S, Dai J, Ding QL, Hu YQ, Wang XF, Deng WW, Wang HL. Zhou RF, et al. Zhonghua Xue Ye Xue Za Zhi. 2005 Nov;26(11):661-4. Zhonghua Xue Ye Xue Za Zhi. 2005. PMID: 16620552 Chinese.

8

A case of factor XI deficiency caused by compound heterozygous F11 gene mutation.

Wang J, Wang X, Dai J, Ding Q, Fu Q, Wang H, Shen L, Li D. Wang J, et al. Among authors: fu q. Haemophilia. 2009 Mar;15(2):603-6. doi: 10.1111/j.1365-2516.2008.01937.x. Haemophilia. 2009. PMID: 19347998

9

Identification of four novel EXT1 and EXT2 mutations in five Chinese pedigrees with hereditary multiple exostoses.

Li Y, Wang D, Wang W, Wang J, Li H, Wang J, Wang X, Fu Q. Li Y, et al. Among authors: fu q. Genet Test Mol Biomarkers. 2009 Dec;13(6):825-30. doi: 10.1089/gtmb.2009.0083. Genet Test Mol Biomarkers. 2009. PMID: 19839753

10

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

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