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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
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  • 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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  • 3. [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 10; 17(4):1021-5. PubMed ID: 19698251
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  • 4. [Mutation analysis of a FGG gene causing hereditary abnormal fibrinogen].
    Jiang L, Zhang Q, Xu W, Zhang Y.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Dec 10; 35(6):812-814. PubMed ID: 30512152
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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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  • 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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  • 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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  • 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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