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 *

224 related articles for article (PubMed ID: 7995928)

  • 1. 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]  

  • 2. Carrier detection in Japanese hemophilia A by use of three intragenic and two extragenic factor VIII DNA probes: a study of 24 kindreds.
    Suehiro K; Tanimoto M; Hamaguchi M; Kojima T; Takamatsu J; Ogata K; Kamiya T; Saito H
    J Lab Clin Med; 1988 Sep; 112(3):314-8. PubMed ID: 2900870
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. Female haemophilia A in a family with seeming extreme bidirectional lyonization tendency: abnormal premature X-chromosome inactivation?
    Ingerslev J; Schwartz M; Lamm LU; Kruse TA; Bukh A; Stenbjerg S
    Clin Genet; 1989 Jan; 35(1):41-8. PubMed ID: 2564325
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genetic mapping and diagnosis of haemophilia A achieved through a BclI polymorphism in the factor VIII gene.
    Gitschier J; Drayna D; Tuddenham EG; White RL; Lawn RM
    Nature; 1985 Apr 25-May 1; 314(6013):738-40. PubMed ID: 2986011
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Carrier detection in hemophilia using pedigree analysis coagulation tests and DNA probes.
    de la Salle C; Baas MJ; Grunebaum L; Wiesel ML; Blanco A; Gialeraki R; Mandalaki T; Cazenave JP
    Nouv Rev Fr Hematol (1978); 1989; 31(3):193-202. PubMed ID: 2575737
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Studies to detect carriers of haemophilia A in German shepherd dogs using diagnostic DNA polymorphisms in the human factor VIII gene.
    Clark P; Bowden DK; Parry BW
    Vet J; 1997 Jan; 153(1):71-4. PubMed ID: 9125358
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A new marker at DXS 115 useful for carrier detection in hemophilia A.
    Wehnert M; Schröder W; Herrmann FH
    Hum Genet; 1990 Nov; 86(1):59-60. PubMed ID: 1979307
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Gene diagnosis of hemophilia A].
    Shen Y
    Zhonghua Yi Xue Za Zhi; 1989 Aug; 69(8):422-6, 30. PubMed ID: 2575928
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Factor VIII gene mutations and RFLP analysis in hemophilia A.
    Krepelová A; Brdicka R; Vorlová Z
    Stem Cells; 1993 May; 11 Suppl 1():72-6. PubMed ID: 8100465
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Factor VIII gene polymorphisms in North Indian population: a consensus algorithm for carrier analysis of hemophilia A.
    Srinivasan A; Mukhopadhyay S; Karim Z; Gupta RK; Gupta A; Wadhawan V; Shukla J; Singh VP; Dash D
    Clin Chim Acta; 2002 Nov; 325(1-2):177-81. PubMed ID: 12367784
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Hemophilia A: carrier detection and prenatal diagnosis by DNA analysis.
    Pecorara M; Casarino L; Mori PG; Morfini M; Mancuso G; Scrivano AM; Boeri E; Molinari AC; De Biasi R; Ciavarella N
    Blood; 1987 Aug; 70(2):531-5. PubMed ID: 3111562
    [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. 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]  

  • 18. Factor VIII gene rearrangement in hemophilia A carrier detection: a word of caution.
    Peretz H; Usher S; Martinovitz U; Seligsohn U
    Blood; 1994 Aug; 84(4):1351-2. PubMed ID: 7914105
    [No Abstract]   [Full Text] [Related]  

  • 19. [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]  

  • 20. Diagnosis of hemophilia A in a female subject by using restriction fragment length polymorphisms linked to the factor VIII gene.
    Randi AM; Sacchi E; Sampietro M; Papaleo G; Muleo G; Mannucci PM
    Ric Clin Lab; 1989; 19(1):75-9. PubMed ID: 2569759
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.