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Journal Abstract Search

364 related items for PubMed ID: 15793786

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  • 3. Identification of three FGA mutations in two Chinese families with congenital afibrinogenaemia.
    Fang Y, Dai BT, Wang XF, Fu QH, Dai J, Xie F, Cai XH, Wang HL, Wang ZY.
    Haemophilia; 2006 Nov; 12(6):615-20. PubMed ID: 17083511
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  • 4. [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; 13(6):1086-9. PubMed ID: 16403286
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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; 31(3):154-6. PubMed ID: 20510102
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  • 7. [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; 34(3):190-4. PubMed ID: 23683413
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  • 8. [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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  • 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; 21(6):846-51. PubMed ID: 25982359
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