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

337 related items for PubMed ID: 8602635

  • 1. 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]

  • 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. Molecular analysis of hemophilia B in Poland: 12 novel mutations of the factor IX gene.
    Wulff K, Bykowska K, Lopaciuk S, Herrmann FH.
    Acta Biochim Pol; 1999 Dec; 46(3):721-6. PubMed ID: 10698280
    [Abstract] [Full Text] [Related]

  • 4. 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; 73(5):774-8. PubMed ID: 7482402
    [Abstract] [Full Text] [Related]

  • 5. 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]

  • 6. Hemophilia B carrier determination based on family-specific mutation detection by DNA single-strand conformation analysis.
    Poon MC, Anand S, Fraser BM, Hoar DI, Sinclair GD.
    J Lab Clin Med; 1993 Jul 01; 122(1):55-63. PubMed ID: 8320491
    [Abstract] [Full Text] [Related]

  • 7. [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 01; 29(3):179-82. PubMed ID: 18788618
    [Abstract] [Full Text] [Related]

  • 8. Six novel and three recurrent mutations in nine Austrian patients with hemophilia B.
    Walter J, Pabinger-Fasching I, Watzke HH.
    Thromb Haemost; 1994 Jul 01; 72(1):74-7. PubMed ID: 7974379
    [Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. 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]

  • 11. Three distinct point mutations in the factor IX gene of three Japanese CRM+ hemophilia B patients (factor IX BMNagoya 2, factor IX Nagoya 3 and 4).
    Hamaguchi M, Matsushita T, Tanimoto M, Takahashi I, Yamamoto K, Sugiura I, Takamatsu J, Ogata K, Kamiya T, Saito H.
    Thromb Haemost; 1991 May 06; 65(5):514-20. PubMed ID: 1871712
    [Abstract] [Full Text] [Related]

  • 12. Identification of mutations in the F9 gene including exon deletion by multiplex ligation-dependent probe amplification in 33 unrelated Korean patients with haemophilia B.
    Kwon MJ, Yoo KY, Kim HJ, Kim SH.
    Haemophilia; 2008 Sep 06; 14(5):1069-75. PubMed ID: 18624698
    [Abstract] [Full Text] [Related]

  • 13. 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 Sep 06; 13(2):160-5. PubMed ID: 10094553
    [Abstract] [Full Text] [Related]

  • 14. Detection of carrier status of hemophilia B using DNA markers.
    Ishak R, Zakaria Z.
    Southeast Asian J Trop Med Public Health; 1997 Sep 06; 28(3):629-30. PubMed ID: 9561621
    [Abstract] [Full Text] [Related]

  • 15. 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 06; 82(5):1437-42. PubMed ID: 10595634
    [Abstract] [Full Text] [Related]

  • 16. Molecular analyses in hemophilia B families: identification of six new mutations in the factor IX gene.
    Espinós C, Casaña P, Haya S, Cid AR, Aznar JA.
    Haematologica; 2003 Feb 06; 88(2):235-6. PubMed ID: 12604421
    [No Abstract] [Full Text] [Related]

  • 17. [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 06; 19(3):125-8. PubMed ID: 11243142
    [Abstract] [Full Text] [Related]

  • 18. 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 06; 90(5):635-42. PubMed ID: 15921378
    [Abstract] [Full Text] [Related]

  • 19. 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]

  • 20. [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]

    Page: [Next] [New Search]
    of 17.