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 *

121 related articles for article (PubMed ID: 1967212)

  • 1. Variation of the non-factor VIII sequences detected by a probe from intron 22 of the factor VIII gene.
    Lillicrap DP; Taylor SA; Schuringa PC; Blanchette VS; Lovsted JK; Weiler LJ; Bridge PJ
    Blood; 1990 Jan; 75(1):139-43. PubMed ID: 1967212
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Carrier detection of ovine hemophilia A using an RFLP marker, and mapping of the factor VIII gene on the ovine X-chromosome.
    Backfisch W; Neuenschwander S; Giger U; Stranzinger G; Pliska V
    J Hered; 1994; 85(6):474-8. PubMed ID: 7995928
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Variant of intron 22 inversions in the factor VIII gene in severe hemophilia A.
    Yamazaki E; Mohri H; Inaba H; Harano H; Kanamori H; Okubo T
    Blood Coagul Fibrinolysis; 1997 Oct; 8(7):445-9. PubMed ID: 9391727
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Diagnosis of hemophilia A carrier state using analysis of intergenic and intergenic polymorphism of factor VIII gene].
    Sawecka J; Strzyga P; Klukowska A; Rokicka-Milewska R; Kościelak J
    Pol Arch Med Wewn; 1995 Nov; 94(5):425-31. PubMed ID: 8833940
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Multiple XbaI polymorphisms for carrier detection and prenatal diagnosis of haemophilia A.
    Chan V; Tong TM; Chan TP; Tang M; Wan CW; Chan FY; Chu YC; Chan TK
    Br J Haematol; 1989 Dec; 73(4):497-500. PubMed ID: 2575402
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A new HindIII restriction fragment length polymorphism in the hemophilia A locus.
    Ahrens P; Kruse TA; Schwartz M; Rasmussen PB; Din N
    Hum Genet; 1987 Jun; 76(2):127-8. PubMed ID: 2886419
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Intron 22-specific long PCR for the Xba I polymorphism in the factor VIII gene.
    El-Maarri O; Oldenburg J; Cağlayan SH
    Br J Haematol; 1999 Jun; 105(4):1120-2. PubMed ID: 10554830
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Hemophilia A: analysis of intron 18 and intron 7 of factor VIII gene and their role in a diagnostic strategy for carrier detection in a Chilean population].
    Quiroga T; Goycoolea M; Kaltwasser G; Morales M; Vildósola J; Muñoz B; Pereira J; Mezzano D
    Rev Med Chil; 1996 Jul; 124(7):777-84. PubMed ID: 9138364
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. A new polymorphism in the factor VIII gene for prenatal diagnosis of hemophilia A.
    Wion KL; Tuddenham EG; Lawn RM
    Nucleic Acids Res; 1986 Jun; 14(11):4535-42. PubMed ID: 3012474
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Simple and convenient detection of a HindIII polymorphic site in intron 19 of factor VIII using PCR.
    Surin VL; Zhukova EL; Krutov AA; Solovyev GYa ; Grineva NI
    Nucleic Acids Res; 1990 Jun; 18(11):3432. PubMed ID: 1972572
    [No Abstract]   [Full Text] [Related]  

  • 13. Haemophilia A in a female: study of a family using intragenic and extragenic restriction site polymorphisms.
    Piétu G; Thomas-Maison N; Sié P; Larrieu MJ; Meyer D
    Thromb Haemost; 1988 Aug; 60(1):102-6. PubMed ID: 2903574
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Partial deletions of factor VIII gene as molecular diagnostic markers in haemophilia A.
    Wehnert M; Herrmann FH; Wulff K
    Dis Markers; 1989; 7(2):113-7. PubMed ID: 2567219
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [XbaI polymorphism in intron 22 of factor VIII and gene potential for prenatal diagnosis of hemophilia A].
    Shen Y
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1990 Aug; 12(4):281-5. PubMed ID: 1979254
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Investigation of factor VIII:C gene restriction fragment length polymorphisms and search for deletions in hemophiliac subjects in Algeria.
    Nafa K; Meriane F; Reghis A; Benabadji M; Demenais F; Guilloud-Bataille M; Sultan Y; Kaplan JC; Delpech M
    Hum Genet; 1990 Apr; 84(5):401-5. PubMed ID: 1969840
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The CpG island in intron 22 of the factor VIII gene is predominantly methylated on the X chromosome of human males.
    De Brasi CD; Bowen DJ; Collins PW; Larripa IB
    J Hum Genet; 2002; 47(5):239-42. PubMed ID: 12032591
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A deletion/insertion leading to the generation of a direct repeat as a result of slipped mispairing and intragenic recombination in the factor VIII gene.
    Tavassoli K; Eigel A; Horst J
    Hum Genet; 1999 May; 104(5):435-7. PubMed ID: 10394938
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The molecular genetic analysis of haemophilia A; characterization of six partial deletions in the factor VIII gene.
    Millar DS; Steinbrecher RA; Wieland K; Grundy CB; Martinowitz U; Krawczak M; Zoll B; Whitmore D; Stephenson J; Mibashan RS
    Hum Genet; 1990 Dec; 86(2):219-27. PubMed ID: 2125022
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 7.