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Journal Abstract Search

234 related items for PubMed ID: 8242057

  • 1. Detection of missense mutations by single-strand conformational polymorphism (SSCP) analysis in five dysfunctional variants of coagulation factor VII.
    Takamiya O, Kemball-Cook G, Martin DM, Cooper DN, von Felten A, Meili E, Hann I, Prangnell DR, Lumley H, Tuddenham EG.
    Hum Mol Genet; 1993 Sep; 2(9):1355-9. PubMed ID: 8242057
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  • 3. Exclusion of the first EGF domain of factor VII by a splice site mutation causes lethal factor VII deficiency.
    McVey JH, Boswell EJ, Takamiya O, Tamagnini G, Valente V, Fidalgo T, Layton M, Tuddenham EG.
    Blood; 1998 Aug 01; 92(3):920-6. PubMed ID: 9680360
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  • 7. [Molecular analysis of two pedigrees with inherited coagulation factor VII deficiency].
    Liang WL, Wei HY, Lin FQ, Zhou JL.
    Zhonghua Er Ke Za Zhi; 2012 Nov 01; 50(11):817-20. PubMed ID: 23302610
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  • 9. Molecular analysis of the genotype-phenotype relationship in factor VII deficiency.
    Millar DS, Kemball-Cook G, McVey JH, Tuddenham EG, Mumford AD, Attock GB, Reverter JC, Lanir N, Parapia LA, Reynaud J, Meili E, von Felton A, Martinowitz U, Prangnell DR, Krawczak M, Cooper DN.
    Hum Genet; 2000 Oct 01; 107(4):327-42. PubMed ID: 11129332
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  • 15. Molecular characterization of four novel mutations causing factor VII deficiency.
    Tamary H, Fromovich-Amit Y, Shalmon L, Zaizov R, Yaniv I, Klar A, Peretz H, Brenner B, Lanir N, Zivelin A, Seligsohn U.
    Hematol J; 2000 Oct 01; 1(6):382-9. PubMed ID: 11920218
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  • 16. Novel mutations in the Factor VII gene of Taiwanese Factor VII-deficient patients.
    Shen MC, Lin JS, Lin SW, Yang WS, Lin B.
    Br J Haematol; 2001 Mar 01; 112(3):566-71. PubMed ID: 11260055
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