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Journal Abstract Search

226 related items for PubMed ID: 31515786

  • 1.
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  • 2. [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; 31(2):134-9. PubMed ID: 24711018
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  • 4. [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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  • 6. [Inherited dysfibrinogenemia caused by Arg16His mutation in alpha chain of fibrinogen.].
    Zhao XJ, Wang ZY, Jiang MH, Zhang W, Cao LJ, Ma ZN, Dong NZ, Bai X, Yu ZQ, Ruan CG.
    Zhonghua Xue Ye Xue Za Zhi; 2010 Mar 10; 31(3):154-6. PubMed ID: 20510102
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  • 8. [A Family with Congenital Dysfibrinogenemia and Blood Transfusion].
    Liao XC, Zhang SS, Yang ZJ, Zhu CL, Huang HN, Luo RX, Li SN, Xie HQ, Li HL, Mo ZN.
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2023 Oct 10; 31(5):1469-1474. PubMed ID: 37846702
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  • 11. [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
    [Abstract] [Full Text] [Related]

  • 12. [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 10; 26(3):133-6. PubMed ID: 15946522
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  • 14. [Congenital afibrinogenemia caused by a novel insertion mutation in the FGB gene].
    Zhang J, Zhao XJ, Wang ZY, Yu ZQ, Cao LJ, Ma ZN, Zhang J, Zhang W, Bai X, Ruan CG.
    Zhonghua Xue Ye Xue Za Zhi; 2013 Sep 10; 34(9):751-6. PubMed ID: 24103871
    [Abstract] [Full Text] [Related]

  • 15. [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
    [Abstract] [Full Text] [Related]

  • 16. [Genetic analysis of an inherited afibrinogenemia family caused by a novel frameshift mutation in FGA].
    Xue F, Ge J, Gu DS, DU WT, Sui T, Zhao HF, Zhang L, Yang RC.
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2009 Aug 14; 17(4):1021-5. PubMed ID: 19698251
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  • 18. [Pathogenesis study of inherited dysfibrinogenemia].
    Liao Z, Xu S, Tang H, Xie Y, Duan X, Liu C, Cheng Y, Chen Y, Wang D, Luo M, Tao Z.
    Zhonghua Yi Xue Za Zhi; 2014 Mar 18; 94(10):742-6. PubMed ID: 24844956
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  • 19. [Analysis of a family with congenital dysfibrinogenemia caused by an Arg275His mutation in the gamma chain of fibrinogen].
    Yan J, Deng D, Deng X, Luo M, Cheng P, Liao L, Lin F.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Apr 18; 33(2):160-3. PubMed ID: 27060305
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  • 20. [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 18; 13(6):1086-9. PubMed ID: 16403286
    [Abstract] [Full Text] [Related]

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