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Journal Abstract Search

149 related items for PubMed ID: 35048620

  • 1. [Pedigree Analysis and Diagnosis of Congenital Dysfibrinogenemia: A Case Report].
    Luo J, Duan SR, Wang H.
    Sichuan Da Xue Xue Bao Yi Xue Ban; 2022 Jan; 53(1):171-174. PubMed ID: 35048620
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  • 2. [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
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  • 3. [Genetic Analysis of A Case of Congenital Dysfibrinogenemia Caused by Arg16His Mutation in Exon 2 of FGA].
    Zhang YL, Liu SY, Zhang ZL, Tao XY, Peng XX, Kong YY.
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2017 Oct 10; 25(5):1514-1517. PubMed ID: 29070135
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  • 4. [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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  • 5. [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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  • 13. A novel fibrinogen variant in a Chinese pedigree with congenital dysfibrinogenemia caused by FGA P. Arg38Thr mutation: A case report.
    Cai R, Li Y, Wang W, Gao X, Liu M, Diao Y, Tang Y, Feng Q.
    Medicine (Baltimore); 2018 Oct 10; 97(40):e12697. PubMed ID: 30290666
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  • 19. [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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  • 20. Congenital dysfibrinogenemia in major surgery: A description of four cases and review of the literature.
    Yan J, Luo M, Xiang L, Wu Y, Lin F.
    Clin Chim Acta; 2022 Mar 01; 528():1-5. PubMed ID: 35063457
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