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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

168 related articles for article (PubMed ID: 7959679)

  • 1. Large DNA inversions, deletions, and TaqI site mutations in severe haemophilia A.
    Figueiredo MS; Tavella MH; Simões BP
    Hum Genet; 1994 Nov; 94(5):473-8. PubMed ID: 7959679
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Inversions of the factor VIII gene in Japanese patients with severe hemophilia A.
    Fukuda K; Naka H; Morichika S; Shibata M; Tanaka I; Shima M; Yoshioka A
    Int J Hematol; 2004 Apr; 79(3):303-6. PubMed ID: 15168603
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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; 11(5):481-91. PubMed ID: 16128892
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Screening for inversions in the factor VIII (F8) gene causing severe haemophilia A.
    Millar DS; Kakkar VV; Cooper DN
    Blood Coagul Fibrinolysis; 1994 Apr; 5(2):239-42. PubMed ID: 8054456
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mutations in haemophilia A.
    Schwaab R; Oldenburg J; Tuddenham EG; Brackmann HH; Olek K
    Br J Haematol; 1993 Mar; 83(3):450-8. PubMed ID: 8485051
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Factor VIII gene inversions in severe hemophilia A patients.
    Van de Water NS; Williams R; Nelson J; Browett PJ
    Pathology; 1995 Jan; 27(1):83-5. PubMed ID: 7603762
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Characterisation of two novel large F8 deletions in patients with severe haemophilia A and factor VIII inhibitors.
    Roth L; Marschalek R; Oldenburg J; Oyen F; Schneppenheim R
    Thromb Haemost; 2011 Feb; 105(2):279-84. PubMed ID: 21103668
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Inversions in the factor VIII gene: improvement of carrier detection and prenatal diagnosis in Dutch haemophilia A families.
    Deutz-Terlouw PP; Losekoot M; Olmer R; Pieneman WC; de Vries-v d Weerd S; Briët E; Bakker E
    J Med Genet; 1995 Apr; 32(4):296-300. PubMed ID: 7643361
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Factor VIII gene deletions in haemophilia A patients in Czechoslovakia.
    Krepelová A; Vorlová Z; Zavadil J; Brdicka R
    Br J Haematol; 1992 Jun; 81(2):271-6. PubMed ID: 1643024
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Identification of factor VIII gene mutations in patients with severe haemophilia A in Venezuela: identification of seven novel mutations.
    Albánez S; Ruiz-Sáez A; Boadas A; de Bosch N; Porco A
    Haemophilia; 2011 Sep; 17(5):e913-8. PubMed ID: 21371196
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The molecular genetics of haemophilia A: screening for point mutations in the factor VIII gene using the restriction enzyme TaqI.
    Millar DS; Zoll B; Martinowitz U; Kakkar VV; Cooper DN
    Hum Genet; 1991 Sep; 87(5):607-12. PubMed ID: 1840568
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Screening for mutations in haemophilia A patients by multiplex PCR-SSCP, Southern blotting and RNA analysis: the detection of a genetic abnormality in the factor VIII gene in 30 out of 35 patients.
    Pieneman WC; Deutz-Terlouw PP; Reitsma PH; Briët E
    Br J Haematol; 1995 Jun; 90(2):442-9. PubMed ID: 7794769
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Haemophilia A: database of nucleotide substitutions, deletions, insertions and rearrangements of the factor VIII gene, second edition.
    Tuddenham EG; Schwaab R; Seehafer J; Millar DS; Gitschier J; Higuchi M; Bidichandani S; Connor JM; Hoyer LW; Yoshioka A
    Nucleic Acids Res; 1994 Nov; 22(22):4851-68. PubMed ID: 7984443
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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; 88(7):778-84. PubMed ID: 12857556
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Investigation of the factor VIII intron 22 repeated region (int22h) and the associated inversion junctions.
    Naylor JA; Buck D; Green P; Williamson H; Bentley D; Giannelli F
    Hum Mol Genet; 1995 Jul; 4(7):1217-24. PubMed ID: 8528212
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Molecular analysis of hemophilia A mutations in the Finnish population.
    Levinson B; Lehesjoki AE; de la Chapelle A; Gitschier J
    Am J Hum Genet; 1990 Jan; 46(1):53-62. PubMed ID: 2104741
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Inversions of the factor VIII gene in Swedish patients with severe haemophilia A.
    Ljung R; Sjörin E
    Eur J Haematol; 1995 May; 54(5):310-3. PubMed ID: 7781755
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Site and type of mutations in the factor VIII gene in patients and carriers of haemophilia A.
    Theophilus BD; Enayat MS; Williams MD; Hill FG
    Haemophilia; 2001 Jul; 7(4):381-91. PubMed ID: 11442643
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Factor VIII mutations in 42 Moldovan haemophilia A families, including 12 that are novel.
    Sirocova N; Tsourea V; Vicol M; Barbacar N; Nakaya SM; Thompson AR; Pratt KP
    Haemophilia; 2009 Jul; 15(4):942-51. PubMed ID: 19473408
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.