These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

109 related items for PubMed ID: 7546452

  • 21. [Indirect methods in the genetic diagnosis of hemophilia A].
    Klein I, Tordai A, Nemes L, Sas G, Váradi A.
    Orv Hetil; 1998 Mar 01; 139(9):487-91. PubMed ID: 9528291
    [Abstract] [Full Text] [Related]

  • 22. 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 01; 88(7):778-84. PubMed ID: 12857556
    [Abstract] [Full Text] [Related]

  • 23. Carrier detection and prenatal diagnosis of hemophilia in developing countries.
    Peyvandi F.
    Semin Thromb Hemost; 2005 Nov 01; 31(5):544-54. PubMed ID: 16276463
    [Abstract] [Full Text] [Related]

  • 24.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 25. High-resolution combined linkage physical map of short tandem repeat loci on human chromosome band Xq28 for indirect haemophilia A carrier detection.
    Machado FB, Medina-Acosta E.
    Haemophilia; 2009 Jan 01; 15(1):297-308. PubMed ID: 18752533
    [Abstract] [Full Text] [Related]

  • 26.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 27. Seven novel and four recurrent point mutations in the factor VIII (F8C) gene.
    Bogdanova N, Lemcke B, Markoff A, Pollmann H, Dworniczak B, Eigel A, Horst J.
    Hum Mutat; 2001 Dec 01; 18(6):546. PubMed ID: 11748850
    [Abstract] [Full Text] [Related]

  • 28. [Detection of factor VIII intron 1 inversion in severe haemophilia A].
    Liang Y, Yan ZY, Yan M, Hua BL, Xiao B, Zhao YQ, Liu JZ.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Jun 01; 26(3):323-5. PubMed ID: 19504449
    [Abstract] [Full Text] [Related]

  • 29.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 30.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 31.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 32. 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 01; 11(5):481-91. PubMed ID: 16128892
    [Abstract] [Full Text] [Related]

  • 33.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 34.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 35.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 36.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 37. [Indirect prenatal molecular diagnostic of haemophilia A and B].
    Morales-Machín A, Borjas-Fajardo L, Zabala W, Alvarez F, Fernández E, Zambrano M, Delgado W, Hernández ML, Solis-Añez E, Chacín JA.
    Invest Clin; 2008 Sep 01; 49(3):289-97. PubMed ID: 18846770
    [Abstract] [Full Text] [Related]

  • 38. Genetic counselling, carrier detection, and prenatal diagnosis in hemophilia. A service experience.
    Kaplan J, Chauvet ML, Briard ML, Gazengel C.
    Ann Genet; 1988 Sep 01; 31(4):221-5. PubMed ID: 3265305
    [Abstract] [Full Text] [Related]

  • 39. PCR assay for the inversion causing severe Hemophilia A and its application.
    Liu J, Liu Q, Liang Y, Wang L, Nozary G, Xiao B, Zhu Z, Zhou Y, Liu L, Guan Y, Zhang J, Sommer SS.
    Chin Med J (Engl); 1999 May 01; 112(5):419-23. PubMed ID: 11593511
    [Abstract] [Full Text] [Related]

  • 40.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 6.