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

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

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 4. Carrier detection and prenatal diagnosis in families with haemophilia.
    Shetty S, Ghosh K, Bhide A, Mohanty D.
    Natl Med J India; 2001; 14(2):81-3. PubMed ID: 11396323
    [Abstract] [Full Text] [Related]

  • 5. 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; 79(4):723-6. PubMed ID: 9569180
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. Inversion of intron 22 in isolated cases of severe hemophilia A.
    Tizzano EF, Domènech M, Baiget M.
    Thromb Haemost; 1995 Jan; 73(1):6-9. PubMed ID: 7740498
    [Abstract] [Full Text] [Related]

  • 9. High throughput mutation screening of the factor VIII gene (F8C) in hemophilia A: 37 novel mutations and genotype-phenotype correlation.
    Citron M, Godmilow L, Ganguly T, Ganguly A.
    Hum Mutat; 2002 Oct; 20(4):267-74. PubMed ID: 12325022
    [Abstract] [Full Text] [Related]

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

  • 11. 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; 2002 Jan; 19(1):84. PubMed ID: 11754115
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. Characterization of factor VIII gene inversions using a non-radioactive detection method: a survey of 102 unrelated haemophilia A families from northern France.
    Gaucher C, Mazurier C.
    Nouv Rev Fr Hematol (1978); 1995 Jan; 37(2):131-6. PubMed ID: 7644350
    [Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. Genetic counseling of hemophilia carriers.
    Ljung R, Tedgård U.
    Semin Thromb Hemost; 2003 Feb; 29(1):31-6. PubMed ID: 12640562
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. Accurate prenatal diagnosis with novel polymerase chain reaction primers in a family with sporadic hemophilia A.
    Sarkar G, Evans MI, Kogan S, Lusher J, Sommer SS.
    Obstet Gynecol; 1989 Sep; 74(3 Pt 1):414-7. PubMed ID: 2569705
    [Abstract] [Full Text] [Related]

  • 20. 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
    [Abstract] [Full Text] [Related]

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