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Journal Abstract Search

350 related items for PubMed ID: 27264807

  • 1. [Homozygous missense mutation p.Val298Met of F10 gene causing hereditary coagulation factor X deficiency in a Chinese pedigree].
    Jin Y, Hao X, Cheng X, Yang L, Chen Y, Xie H, Wang Y, Wang M.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Jun; 33(3):296-9. PubMed ID: 27264807
    [Abstract] [Full Text] [Related]

  • 2. [Phenotype and genotype analysis for a consanguineous pedigree with combined coagulation factor VII and X deficiency].
    Jin Y, Wang M, Wang Y, Yang X, Yang L, Xie Y, Xie H, Zhu L, Yu F.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Feb; 31(1):16-20. PubMed ID: 24510554
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  • 3. [Genotypic and phenotypic analysis of a case with inherited coagulation factor X deficiency].
    Chen T, Li F, Shu K, Liu J, Shen C, Zhang Z, Jin S, Wang X, Jiang M.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Aug 10; 35(4):544-547. PubMed ID: 30098253
    [Abstract] [Full Text] [Related]

  • 4. [Gene analysis of a combined inherited factor VII and factor X deficiency pedigree].
    Wang MS, Jin YH, Zheng FX, Xie HX, Xu PF, Niu ZZ.
    Zhonghua Xue Ye Xue Za Zhi; 2011 Dec 10; 32(12):854-7. PubMed ID: 22339961
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  • 5. [Analysis of a consanguineous pedigree featuring hereditary coagulation factor Ⅴ deficiency].
    Xie YS, Zhang Y, Zhu LQ, Jin YH, Yang LH, Xie HX, Wang MS, Yang XL.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Apr 10; 30(2):161-4. PubMed ID: 23568726
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  • 6. Characterization of a homozygous Gly11Val mutation in the Gla domain of coagulation factor X.
    Chafa O, Tagzirt M, Tapon-Bretaudière J, Reghis A, Fischer AM, LeBonniec BF.
    Thromb Res; 2009 May 10; 124(1):144-8. PubMed ID: 19135706
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  • 7. [Inherited coagulation factor X deficiency caused by two novel mutations in factor X gene].
    Wang WB, Wang HL, Wang XF, Fu QH, Zhou RF, Xie S, Hu YQ, Wang ZY.
    Zhonghua Xue Ye Xue Za Zhi; 2004 Sep 10; 25(9):519-22. PubMed ID: 15569527
    [Abstract] [Full Text] [Related]

  • 8. [Analysis of a consanguineous pedigree affected with hereditary coagulation factor XII deficiency caused by homozygous Gly341Arg mutation].
    Yang L, Jin S, Ji W, Cheng X, Li X, Jin Y, Wang M.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Feb 10; 35(1):69-73. PubMed ID: 29419864
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  • 13. A new factor X defect (factor X Padua 3): a compound heterozygous between true deficiency (Gly(380)-->Arg) and an abnormality (Ser(334)-->Pro).
    Vianello F, Lombardi AM, Boldrin C, Luni S, Girolami A.
    Thromb Res; 2001 Nov 15; 104(4):257-64. PubMed ID: 11728527
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  • 16. [Analysis on the novel compound heterozygous mutation FⅪ of a patient with hereditary factor Ⅺ deficiency].
    Xu K, Shu KY, Li FF, Chen T, Liu J, Jin SS, Guo JJ, Zhang ZH, Jiang MH.
    Zhonghua Yi Xue Za Zhi; 2017 Dec 26; 97(48):3774-3778. PubMed ID: 29325334
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  • 17. [Genetic analysis of a pedigree with hereditary coagulation factor Ⅶ deficiency].
    Jin Y, Wang Y, Hao X, Yang L, Xie H, Zhu L, Yu F, Yang X, Wang M.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Apr 26; 32(2):222-5. PubMed ID: 25863091
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  • 18. Severe factor X deficiency in three unrelated Palestinian patients is caused by homozygosity for the mutation c302delG-correlation with thrombin generation and thromboelastometry.
    Livnat T, Shenkman B, Kenet G, Tamarin I, Gillis S, Varon D, Iijima K, Zivelin A, Salomon O.
    Blood Coagul Fibrinolysis; 2011 Dec 26; 22(8):673-9. PubMed ID: 22008904
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  • 19. Impaired prothrombinase activity of factor X Gly381Asp results in severe familial CRM+ FX deficiency.
    Pinotti M, Camire RM, Baroni M, Rajab A, Marchetti G, Bernardi F.
    Thromb Haemost; 2003 Feb 26; 89(2):243-8. PubMed ID: 12574802
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