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

165 related items for PubMed ID: 2149345

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. [Detection of hemophilia A carriers by PCR analysis of hind III polymorphism in the factor VIII gene].
    Wu S, Li Y, Cui H, Xie Y, Zheng J, Pan X, Zhang H, Zhao R, Zhang Q.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1998 Apr 10; 15(2):78-80. PubMed ID: 9531644
    [Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4. Genomic carrier detection and prenatal diagnosis of haemophilia A in families at risk using the polymerase chain reaction (PCR).
    Wehnert M, Shukova EL, Surin VL, Schröder W, Solovjev GYa, Grinjeva NI, Herrmann FH.
    Folia Haematol Int Mag Klin Morphol Blutforsch; 1990 Apr 10; 117(4):617-22. PubMed ID: 1714868
    [Abstract] [Full Text] [Related]

  • 5. Informativeness of linkage analysis for genetic diagnosis of haemophilia A in India.
    Jayandharan G, Shaji RV, George B, Chandy M, Srivastava A.
    Haemophilia; 2004 Sep 10; 10(5):553-9. PubMed ID: 15357783
    [Abstract] [Full Text] [Related]

  • 6. [Analysis of the AluI polymorphism in intron 1 of the human coagulation factor VIII gene: a new marker for the hemophilia A carrier detection].
    Surin VL, Luk'ianenko AV, Luchinina IuA.
    Genetika; 2007 Apr 10; 43(4):560-6. PubMed ID: 17555134
    [Abstract] [Full Text] [Related]

  • 7. [Application studies on the gene diagnosis and carrier detection of hemophilia A by using polymerase chain reaction-conformation sensitive gel electrophoresis].
    Lillicrap D, He GP, Leggo J, Liu YS, Tong XH, Zhou GX, Luo LH.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Aug 10; 26(4):393-9. PubMed ID: 20017302
    [Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. Identification of new dinucleotide-repeat polymorphisms in factor VIII gene using fluorescent PCR.
    Kim JW, Park SY, Kim YM, Kim JM, Kim DJ, Ryu HM.
    Haemophilia; 2005 Jan 10; 11(1):38-42. PubMed ID: 15660987
    [Abstract] [Full Text] [Related]

  • 10. HindIII polymorphism in carrier detection of hemophilia A in India: a new primer design.
    Raza ST, Husain N, Bhatt AN, Avneesh.
    Clin Appl Thromb Hemost; 2007 Oct 10; 13(4):432-4. PubMed ID: 17895514
    [Abstract] [Full Text] [Related]

  • 11. Factor VIII gene haplotypes and linkage disequilibrium for the indirect genetic analysis of hemophilia A in India.
    Singh M, Singh P.
    Clin Appl Thromb Hemost; 2009 Oct 10; 15(3):334-9. PubMed ID: 18160577
    [Abstract] [Full Text] [Related]

  • 12. Application of intron 9 and intron 25 dinucleotide repeats of the factor VIII gene for carrier diagnosis in haemophilia A.
    Venceslá A, Baena M, Fares Taie L, Cornet M, Baiget M, Tizzano EF.
    Haemophilia; 2008 May 10; 14(3):489-93. PubMed ID: 18384354
    [Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. Carrier analysis and prenatal diagnosis of haemophilia A in North India.
    Pandey GS, Phadke SR, Mittal B.
    Int J Mol Med; 2002 Nov 10; 10(5):661-4. PubMed ID: 12373312
    [Abstract] [Full Text] [Related]

  • 15. A rapid multifluorescent polymerase chain reaction for genetic counselling in Chinese haemophilia A families.
    Fang Y, Wang XF, Dai J, Wang HL.
    Haemophilia; 2006 Jan 10; 12(1):62-7. PubMed ID: 16409177
    [Abstract] [Full Text] [Related]

  • 16. [Analysis of X ba I polymorphism of FVIII gene and its application on prenatal diagnosis for hemophilia A].
    Wang ZY, Liang Y, Zhou Y, Xiao B, Liu JZ.
    Zhonghua Xue Ye Xue Za Zhi; 2006 Mar 10; 27(3):170-2. PubMed ID: 16792918
    [Abstract] [Full Text] [Related]

  • 17. Screening for hemophilia A carriers: utility of PCR-RFLP--based polymorphism analysis.
    Tasleem Raza S, Husain N, Kumar A.
    Clin Appl Thromb Hemost; 2009 Feb 10; 15(1):78-83. PubMed ID: 19150994
    [Abstract] [Full Text] [Related]

  • 18. Precise carrier diagnosis in families with haemophilia A: use of conformation sensitive gel electrophoresis for mutation screening and polymorphism analysis.
    Williams IJ, Abuzenadah A, Winship PR, Preston FE, Dolan G, Wright J, Peake IR, Goodeve AC.
    Thromb Haemost; 1998 Apr 10; 79(4):723-6. PubMed ID: 9569180
    [Abstract] [Full Text] [Related]

  • 19. Carrier detection by DNA linkage analysis in eighty Thai hemophilia A families.
    Mahasandana C, Pung-Amritt P, Treesucon A, Petrarat S, Veerakul G, Visudhiphan S, Yenchitsomanus PT.
    J Med Assoc Thai; 2002 Aug 10; 85 Suppl 2():S513-21. PubMed ID: 12403227
    [Abstract] [Full Text] [Related]

  • 20. [Significance of BclI and HindIII polymorphism detection in genetic diagnosis of familial hemophilia A].
    Qiao XQ, Li YP, Zeng L, Chen Y, Han X.
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2011 Feb 10; 19(1):189-92. PubMed ID: 21362249
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 9.