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Journal Abstract Search

231 related items for PubMed ID: 29652987

  • 1. [Analysis of a pedigree affected with congenital hypofibrinogenemia due to heterozygous Ser313Ile mutation of fibrinogen γ chain gene].
    Zhu L, Zhao M, Cheng X, Yu D, Li X, Xu F, Wang J, Wang M.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Apr 10; 35(2):179-183. PubMed ID: 29652987
    [Abstract] [Full Text] [Related]

  • 2. [Congenital hypofibrinogenemia associated with a novel mutation in FGG gene].
    Wang Y, Ding H, Hao X, Zhu L, Yang L, Jin Y, Wang M.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Jun 10; 32(3):331-4. PubMed ID: 26037343
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  • 6. [Inherited afibrinogenemia caused by compound heterozygous mutations in the beta beta-chain of fibrinogen].
    Fang Y, Wang HL, Wang XF, Fu QH, Wang WB, Xie S, Zhou RF, Dai J, Wang ZY.
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2005 Dec 10; 13(6):1086-9. PubMed ID: 16403286
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  • 7. [Genetic analysis of a Chinese pedigree affected with Congenital dysfibrinogenemia due to variant of FGG gene].
    Shao X, Ma J, Wang Z, Sun M, Huang Z, Jiang Z, Liu X, Li S, Liu Y.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Nov 10; 40(11):1324-1329. PubMed ID: 37906135
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  • 8. [A case of inherited afibrinogenemia caused by an IVS7-12A>G splice mutation of FGG gene].
    Wang X, Yang X, Wang J, Shu K, Li F, Yang W, Ruan J, Wang S, Jiang M.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Dec 10; 37(12):1391-1394. PubMed ID: 33306830
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  • 9. [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.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Apr 10; 22(2):201-3. PubMed ID: 15793786
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  • 10. [Clinical and genetic analysis of 8 Chinese pedigrees with inherited dysfibrinogenemia].
    Jiang M, Wang X, Shu K, Jiang W, Huang Y, Lin Y, Li S, Hu Y.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Apr 10; 31(2):134-9. PubMed ID: 24711018
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  • 12. [Fibrinogen gamma-chain mutation, p.Ile171His, leads to hereditary hypofibrinogenemia].
    Liu JX, Wang CJ, Dai JH, Zhang MX, Lyu B, Jiang B.
    Zhonghua Nei Ke Za Zhi; 2022 Feb 01; 61(2):172-176. PubMed ID: 35090252
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  • 14. [Congenital Fibrinogen Deficiency Caused by Novel FGG Gene Mutation].
    Wang TT, Shao JR, Wang J, Cheng Y, Zhang XQ, Fang YH, Yao CF, Zhang XS.
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2021 Apr 01; 29(2):586-590. PubMed ID: 33812435
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  • 15. Novel mutations (γTrp208Leu and γLys232Thr) leading to congenital hypofibrinogenemia in two unrelated Chinese families.
    Zhu L, Wang Y, Zhao M, Hao X, Xie H, Xie Y, Wang M, Ding H.
    Blood Coagul Fibrinolysis; 2014 Dec 01; 25(8):894-7. PubMed ID: 24914742
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  • 16. [Phenotype and genotype analyses of two pedigrees with inherited fibrinogen deficiency].
    Jia KQ, Su ZX, Chen HL, Zheng XY, Zeng ML, Zhang K, Ye LY, Yang LL, Jin YH, Wang MS.
    Zhonghua Xue Ye Xue Za Zhi; 2023 Nov 14; 44(11):930-935. PubMed ID: 38185523
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  • 18. [Functional study of abnormal fibrinogen caused by Arg275His mutation in fibrinogen γ chain].
    Zhou JY, Wang XF, Ding QL, Xu GQ, Zhang LW, Dai J, Lu YL, Xi XD, Wang HL.
    Zhonghua Xue Ye Xue Za Zhi; 2013 Mar 14; 34(3):190-4. PubMed ID: 23683413
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  • 19. Congenital afibrinogenemia: Identification and characterization of two novel homozygous fibrinogen Aα and Bβ chain mutations in two Tunisian families.
    Amri Y, Toumi Nel H, Hadj Fredj S, de Moerloose P.
    Thromb Res; 2016 Jul 14; 143():11-6. PubMed ID: 27164460
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  • 20. [Congenital afibrinogenemia associated with a novel nonsense mutation in the FGA gene].
    Wu SY, Wang ZY, Dong NZ, Bai X, Ruan CG.
    Zhonghua Xue Ye Xue Za Zhi; 2005 Mar 14; 26(3):133-6. PubMed ID: 15946522
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