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Journal Abstract Search

342 related items for PubMed ID: 12015062

  • 1. [Identification of two novel mutation in two Chinese hereditary coagulation factor XIII deficiency families].
    Duan B, Wang H, Chu H, Wang X, Qu B, Li D, Wang H, Yin J, Kang W, Wang Z.
    Zhonghua Xue Ye Xue Za Zhi; 2002 Mar; 23(3):117-20. PubMed ID: 12015062
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  • 2. [Identification of a novel mutation of F (13) A gene in a pedigree with factor XIII deficiency].
    Jiao WY, Wu JS, Ding QL, Wang XF, Xu XC, Ding KY, Liu X.
    Zhonghua Xue Ye Xue Za Zhi; 2007 Sep; 28(9):598-601. PubMed ID: 18246815
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  • 6. Congenital factor XIII deficiency caused by two mutations in eight Tunisian families: molecular confirmation of a founder effect.
    Louhichi N, Medhaffar M, Hadjsalem I, Mkaouar-Rebai E, Fendri-Kriaa N, Kanoun H, Yaïch F, Souissi T, Elloumi M, Fakhfakh F.
    Ann Hematol; 2010 May; 89(5):499-504. PubMed ID: 19937244
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  • 8. Phenotype-genotype correlation in eight Polish patients with inherited Factor XIII deficiency: identification of three novel mutations.
    Ivaskevicius V, Windyga J, Baran B, Schroeder V, Junen J, Bykowska K, Seifried E, Kohler HP, Oldenburg J.
    Haemophilia; 2007 Sep; 13(5):649-57. PubMed ID: 17880458
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  • 9. Congenital factor XIII deficiency in Pakistan: characterization of seven families and identification of four novel mutations.
    Borhany M, Handrkova H, Cairo A, Schroeder V, Fatima N, Naz A, Amanat S, Shamsi T, Peyvandi F, Kohler HP.
    Haemophilia; 2014 Jul; 20(4):568-74. PubMed ID: 24329762
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  • 13. Molecular modeling predicts structural changes in the A subunit of factor XIII caused by two novel mutations identified in a neonate with severe congenital factor XIII deficiency.
    Souri M, Yee VC, Fujii N, Ichinose A.
    Thromb Res; 2012 Sep; 130(3):506-10. PubMed ID: 22633530
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  • 16. [The inherited coagulation factor XI deficiency caused by intronic mutation IVS J-4delgttg].
    Xie S, Wang HL, Wang XF, Wu WM, Zhou RF, Wang WB, Hu YQ, Wang ZY.
    Zhonghua Xue Ye Xue Za Zhi; 2005 Mar; 26(3):144-7. PubMed ID: 15946525
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  • 17. Factor XIII deficiency: complete phenotypic characterization of two cases with novel causative mutations.
    Katona É, Muszbek L, Devreese K, Kovács KB, Bereczky Z, Jonkers M, Shemirani AH, Mondelaers V, Ermens AA.
    Haemophilia; 2014 Jan; 20(1):114-20. PubMed ID: 24118344
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  • 19. [Novel double heterozygous mutations on Met306Val and Thr181Asn related to a hereditary coagulation factor VII deficiency].
    Tu CQ, Deng CY, Wu JZ, Pan CY, Xie CY.
    Zhonghua Yi Xue Za Zhi; 2006 Jan 10; 86(2):124-7. PubMed ID: 16620721
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