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Journal Abstract Search

126 related items for PubMed ID: 37516116

  • 1. A Novel Fibrinogen Mutation p.BβAla68Asp Causes an Inherited Dysfibrinogenemia.
    Jia K, Zeng M, Zheng X, Xie H, Yang L, Xie Y, Wang M.
    Hamostaseologie; 2023 Dec; 43(6):426-431. PubMed ID: 37516116
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  • 2. Analysis of an Inherited Dysfibrinogenemia Pedigree Associated with a Heterozygous Mutation in the FGA Gene.
    Li S, Wang M, Li X, Xu Q, Liu S, Luo S, Chen Y.
    Hamostaseologie; 2020 Dec; 40(5):642-648. PubMed ID: 33374030
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  • 3. [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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  • 4. Phenotypic and genetic analysis of hypofibrinogenemia because of a novel missense mutation in the FGB: Leu121Arg.
    Zhang H, Luo S, Fang W, Liu S, Su K, Yang L, Jin Y, Wang M.
    Blood Coagul Fibrinolysis; 2019 Jul 14; 30(5):233-238. PubMed ID: 31259773
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  • 5. A novel heterozygous mutation (γIIe367Thr) causes congenital dysfibrinogenemia in a Chinese family.
    Luo S, Xu Q, Xie Y, Li X, Jin Y, Yang L, Liu S, Wang M.
    Blood Coagul Fibrinolysis; 2020 Dec 14; 31(8):569-574. PubMed ID: 32833807
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  • 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.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Apr 14; 22(2):201-3. PubMed ID: 15793786
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  • 8. [Analysis of a pedigree affected with congenital dysfibrinogenemia due to a novel Gly31Glu mutation of FGA gene].
    Wang X, Yang X, Yang W, Shu K, Li F, Liu J, Zhang Z, Li S, Jiang M.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Sep 10; 36(9):901-904. PubMed ID: 31515786
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  • 10. [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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  • 18. Coexisting congenital dysfibrinogenemia with a novel mutation in fibrinogen γ chain (γ322 Phe→Ile, Fibrinogen Beijing) and haemophilia B in a family.
    Hua B, Li K, Lee A, Poon MC, Zhao Y.
    Haemophilia; 2015 Nov 10; 21(6):846-51. PubMed ID: 25982359
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  • 19. [Genetic analysis of two Chinese pedigrees affected with Hereditary hypofibrinemia due to missense variants].
    Zheng X, Chen Y, Wen M, Jin Y, Zeng M, Jia K, Chen Y, Wang M, Yang L.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Mar 10; 40(3):276-281. PubMed ID: 36854400
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