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Journal Abstract Search

385 related items for PubMed ID: 10698280

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

  • 2. Molecular characterization of hemophilia B in North Indian families: identification of novel and recurrent molecular events in the factor IX gene.
    Mahajan A, Chavali S, Kabra M, Chowdhury MR, Bharadwaj D.
    Haematologica; 2004 Dec; 89(12):1498-503. PubMed ID: 15590401
    [Abstract] [Full Text] [Related]

  • 3. Heteroduplex analysis in hemophilia B: detection of two novel factor IX gene mutations.
    Driscoll MC, Chu A, Hilgartner MW.
    Am J Hematol; 1996 Apr; 51(4):324-7. PubMed ID: 8602635
    [Abstract] [Full Text] [Related]

  • 4. Molecular genotyping of the Italian cohort of patients with hemophilia B.
    Belvini D, Salviato R, Radossi P, Pierobon F, Mori P, Castaldo G, Tagariello G, AICE HB Study Group.
    Haematologica; 2005 May; 90(5):635-42. PubMed ID: 15921378
    [Abstract] [Full Text] [Related]

  • 5. Factor IX gene analysis in 70 unrelated patients with haemophilia B: description of 13 new mutations.
    Attali O, Vinciguerra C, Trzeciak MC, Durin A, Pernod G, Gay V, Ménart C, Sobas F, Dechavanne M, Négrier C.
    Thromb Haemost; 1999 Nov; 82(5):1437-42. PubMed ID: 10595634
    [Abstract] [Full Text] [Related]

  • 6. Genetic basis and carrier detection of hemophilia B of Chinese origin.
    Lin SW, Shen MC.
    Thromb Haemost; 1993 Mar 01; 69(3):247-52. PubMed ID: 8470048
    [Abstract] [Full Text] [Related]

  • 7. Detection of ten new mutations by screening the gene encoding factor IX of Danish hemophilia B patients.
    Nielsen LR, Scheibel E, Ingerslev J, Schwartz M.
    Thromb Haemost; 1995 May 01; 73(5):774-8. PubMed ID: 7482402
    [Abstract] [Full Text] [Related]

  • 8. Identification of twenty-one new mutations in the factor IX gene by SSCP analysis.
    Montejo JM, Magallón M, Tizzano E, Solera J.
    Hum Mutat; 1999 May 01; 13(2):160-5. PubMed ID: 10094553
    [Abstract] [Full Text] [Related]

  • 9. Spectrum of factor IX gene mutations causing haemophilia B from India.
    Ghosh K, Quadros L, Shetty S.
    Blood Coagul Fibrinolysis; 2009 Jul 01; 20(5):333-6. PubMed ID: 19357501
    [Abstract] [Full Text] [Related]

  • 10. Novel mutations in factor IX gene from western India with reference to their phenotypic and haplotypic attributes.
    Quadros L, Ghosh K, Shetty S.
    J Pediatr Hematol Oncol; 2009 Mar 01; 31(3):157-60. PubMed ID: 19262239
    [Abstract] [Full Text] [Related]

  • 11. Molecular analysis of factor IX gene in an Iranian female with severe hemophilia B.
    Karimipoor M, Kokabee L, Kamali E, Karizi SZ, Zeinali S.
    Acta Haematol; 2008 Mar 01; 119(3):151-3. PubMed ID: 18434706
    [Abstract] [Full Text] [Related]

  • 12. Point mutations in four hemophilia B patients from China.
    Wang NS, Chen SH, Thompson AR.
    Thromb Haemost; 1990 Oct 22; 64(2):302-6. PubMed ID: 2270538
    [Abstract] [Full Text] [Related]

  • 13. Fast and efficient mutation detection method using multiplex PCR and cycle sequencing--application to haemophilia B.
    Costa JM, Ernault P, Vidaud D, Vidaud M, Meyer D, Lavergne JM.
    Thromb Haemost; 2000 Feb 22; 83(2):244-7. PubMed ID: 10739381
    [Abstract] [Full Text] [Related]

  • 14. [Molecular diagnosis of inherited coagulation disorders--sequence analysis of hemophilia B patients with anti-factor IX antibodies].
    Tanimoto M, Matsushita T, Takamatsu J, Saito H.
    Rinsho Byori; 1990 Sep 22; 38(9):1041-6. PubMed ID: 2232265
    [Abstract] [Full Text] [Related]

  • 15. [Four novel point mutations of factor IX gene detected by denaturing gradient gel electrophoresis].
    Wang Y, Li Z, Wan H.
    Zhonghua Xue Ye Xue Za Zhi; 1998 Mar 22; 19(3):125-8. PubMed ID: 11243142
    [Abstract] [Full Text] [Related]

  • 16. Two mutations of the factor IX gene including a donor splice consensus deletion and a point mutation in a Dutch patient with severe hemophilia B.
    Poort SR, Briët E, Bertina RM, Reitsma PH.
    Thromb Haemost; 1990 Nov 30; 64(3):379-84. PubMed ID: 2096489
    [Abstract] [Full Text] [Related]

  • 17. Five novel point mutations: two causing haemophilia B and three causing factor X deficiency.
    Odom MW, Leone G, De Stefano V, Montiel MM, Boland EJ, Anderson J, Jagadeeswaran P.
    Mol Cell Probes; 1994 Feb 30; 8(1):63-5. PubMed ID: 8028609
    [Abstract] [Full Text] [Related]

  • 18. Haplotype analysis of identical factor IX mutants using PCR.
    Green PM, Montandon AJ, Ljung R, Nilsson IM, Giannelli F.
    Thromb Haemost; 1992 Jan 23; 67(1):66-9. PubMed ID: 1615486
    [Abstract] [Full Text] [Related]

  • 19. [Gene diagnosis of 3 haemophilia B families].
    Zhang Y, Yang LH, Lu YL, Ding QL, Wang XF, Liu XE, Zhang L.
    Zhonghua Xue Ye Xue Za Zhi; 2008 Mar 23; 29(3):179-82. PubMed ID: 18788618
    [Abstract] [Full Text] [Related]

  • 20. Identification of factor IX mutations in Iranian haemophilia B patients by SSCP and sequencing.
    Karimipoor M, Zeinali S, Nafissi N, Tuddenham EG, Lak M, Safaee R.
    Thromb Res; 2007 Mar 23; 120(1):135-9. PubMed ID: 17014892
    [Abstract] [Full Text] [Related]

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