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Journal Abstract Search

132 related items for PubMed ID: 7644350

  • 1.
    ; . PubMed ID:
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  • 2. Analysis of large structural changes of the factor VIII gene, involving intron 1 and 22, in severe hemophilia A.
    Andrikovics H, Klein I, Bors A, Nemes L, Marosi A, Váradi A, Tordai A.
    Haematologica; 2003 Jul; 88(7):778-84. PubMed ID: 12857556
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  • 3. [Molecular genetics of hemophilia A].
    De Brasi CD, Slavutsky IR, Larripa IB.
    Medicina (B Aires); 1996 Jul; 56(5 Pt 1):509-17. PubMed ID: 9239887
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  • 4. Clinical correlates among 49 families with hemophilia A and factor VIII gene inversions.
    Weinmann AF, Schoof JM, Thompson AR.
    Am J Hematol; 1996 Mar; 51(3):192-9. PubMed ID: 8619399
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  • 5. [Intron 1 and 22 inversions in factor VIII gene in patients with haemophilia A].
    Li T, Dai J, Wu JS, Ding QL, Ding KY, Zheng CC, Sun P, Wang XF.
    Zhonghua Xue Ye Xue Za Zhi; 2009 Mar; 30(3):150-3. PubMed ID: 19642360
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  • 7. Factor VIII gene rearrangement analysis and carrier determination in hemophilia A.
    Poon MC, Low S, Sinclair GD.
    J Lab Clin Med; 1995 Mar; 125(3):402-6. PubMed ID: 7897307
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  • 8. Inversions disrupting the factor VIII gene are a common cause of severe haemophilia A.
    Lakich D, Kazazian HH, Antonarakis SE, Gitschier J.
    Nat Genet; 1993 Nov; 5(3):236-41. PubMed ID: 8275087
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  • 11. Carrier detection and prenatal diagnosis in families with haemophilia.
    Shetty S, Ghosh K, Bhide A, Mohanty D.
    Natl Med J India; 2001 Nov; 14(2):81-3. PubMed ID: 11396323
    [Abstract] [Full Text] [Related]

  • 12. Inversion mutation as a major cause of severe hemophilia A in Italian patients.
    Mori PG, Caprino D, Bicocchi MP, Valetto A, Bottini F, Aquila M.
    Haematologica; 1997 Nov; 82(1):75-6. PubMed ID: 9107090
    [Abstract] [Full Text] [Related]

  • 13. Inversions of the factor VIII gene in Japanese patients with severe hemophilia A.
    Fukuda K, Naka H, Morichika S, Shibata M, Tanaka I, Shima M, Yoshioka A.
    Int J Hematol; 2004 Apr; 79(3):303-6. PubMed ID: 15168603
    [Abstract] [Full Text] [Related]

  • 14. Inversions in the factor VIII gene: improvement of carrier detection and prenatal diagnosis in Dutch haemophilia A families.
    Deutz-Terlouw PP, Losekoot M, Olmer R, Pieneman WC, de Vries-v d Weerd S, Briët E, Bakker E.
    J Med Genet; 1995 Apr; 32(4):296-300. PubMed ID: 7643361
    [Abstract] [Full Text] [Related]

  • 15. Prevalence of the intron 22 inversion of the factor VIII gene and inhibitor development in Polish patients with severe hemophilia A.
    Sawecka J, Skulimowska J, Windyga J, Lopaciuk S, Kościelak J.
    Arch Immunol Ther Exp (Warsz); 2005 Apr; 53(4):352-6. PubMed ID: 16088320
    [Abstract] [Full Text] [Related]

  • 16. Spectrum of factor VIII mutations in Arab patients with severe haemophilia A.
    Abu-Amero KK, Hellani A, Al-Mahed M, Al-Sheikh I.
    Haemophilia; 2008 May; 14(3):484-8. PubMed ID: 18371166
    [Abstract] [Full Text] [Related]

  • 17. [Molecular biologic study and the factor VIII gene in hemophilia A].
    Bock I, Melegh B, Nagy A, Losonczy H, Csete B, Schröder W, Kardos M, István L, Jager R, Tóth AM, Tóth A, Falko H, Mózsik G.
    Orv Hetil; 1996 Nov 17; 137(46):2573-5. PubMed ID: 9005386
    [Abstract] [Full Text] [Related]

  • 18. Another variant pattern of intron 22 inversion in the factor VIII gene seen in a severe haemophilia A patient.
    Enayat MS, Theophilus BD, Williams MD, Wilde JT, Hill FG.
    Thromb Haemost; 1997 Oct 17; 78(4):1303. PubMed ID: 9365008
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  • 19. Identification of factor VIII gene mutations in 101 patients with haemophilia A: mutation analysis by inversion screening and multiplex PCR and CSGE and molecular modelling of 10 novel missense substitutions.
    Jayandharan G, Shaji RV, Baidya S, Nair SC, Chandy M, Srivastava A.
    Haemophilia; 2005 Sep 17; 11(5):481-91. PubMed ID: 16128892
    [Abstract] [Full Text] [Related]

  • 20. Alport syndrome. Molecular genetic aspects.
    Hertz JM.
    Dan Med Bull; 2009 Aug 17; 56(3):105-52. PubMed ID: 19728970
    [Abstract] [Full Text] [Related]

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