BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

335 related articles for article (PubMed ID: 17555134)

  • 21. Utility of a (GT) dinucleotide repeat in intron 1 of the factor 8 gene for haemophilia A carrier diagnosis.
    Tizzano E; Venceslá A; Cornet M; Baena M; Baiget M
    Haemophilia; 2005 Mar; 11(2):142-4. PubMed ID: 15810916
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Diagnosis of hemophilia A by a combination of St14(DXS52) VNTR polymorphism and (CA)n repeat polymorphism within FVIII gene].
    Zhong CG; Li LY; Lu GX
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Feb; 21(1):80-2. PubMed ID: 14767918
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. 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]  

  • 25. Carrier detection for prenatal diagnosis of hemophilia A in Italian families.
    Cappello N; Restagno G; Garnerone S; Gennaro C; Perugini L; Rendine S; Piazza A; Carbonara A
    Haematologica; 1992; 77(4):302-6. PubMed ID: 1358771
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Nucleotide changes around the splicing acceptor of intron 24 in the factor VIII gene and its impact on splicing.
    Gau JP; Chen CC; Hsu HC; Ho CH; Chau WK; You JY; Yu YB
    Blood Coagul Fibrinolysis; 2006 Jan; 17(1):53-6. PubMed ID: 16607080
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. [Detection of factor VIII intron 1 inversion in severe haemophilia A].
    Liang Y; Yan ZY; Yan M; Hua BL; Xiao B; Zhao YQ; Liu JZ
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Jun; 26(3):323-5. PubMed ID: 19504449
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Mutation screening of the F VIII gene in 10 hemophilia A families].
    LI W; HU X; GAO BD; LI LY; LIAO Y; TANG XM; TANG WL; Lu GX
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Apr; 28(2):127-32. PubMed ID: 21462120
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Screening for hemophilia A carriers: utility of PCR-RFLP--based polymorphism analysis.
    Tasleem Raza S; Husain N; Kumar A
    Clin Appl Thromb Hemost; 2009 Feb; 15(1):78-83. PubMed ID: 19150994
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Factor VIII gene rearrangement analysis and carrier determination in hemophilia A.
    Poon MC; Low S; Sinclair GD
    J Lab Clin Med; 1995 Mar; 125(3):402-6. PubMed ID: 7897307
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Intragenic variable number tandom repeats in coagulation factor VIII gene of Chinese origin].
    Wang XD
    Zhonghua Yi Xue Za Zhi; 1993 Apr; 73(4):206-8, 252. PubMed ID: 8395312
    [TBL] [Abstract][Full Text] [Related]  

  • 33. A rapid multifluorescent polymerase chain reaction for genetic counselling in Chinese haemophilia A families.
    Fang Y; Wang XF; Dai J; Wang HL
    Haemophilia; 2006 Jan; 12(1):62-7. PubMed ID: 16409177
    [TBL] [Abstract][Full Text] [Related]  

  • 34. A novel informative dinucleotide microsatellite marker located on human factor VIII intron 25.
    Machado FB; Duarte LP; Medina-Acosta E
    Haemophilia; 2009 Mar; 15(2):613-4. PubMed ID: 19187187
    [No Abstract]   [Full Text] [Related]  

  • 35. Polymorphism distribution of Int13, Int22, and St14 VNTRs in a Mexican population and their application in carrier diagnosis of hemophilia A.
    Gallegos RM; Aranda HB; Navarrete CP; Espinoza R; Gómez FS; Aranda DA
    Am J Hematol; 2004 Sep; 77(1):1-6. PubMed ID: 15307098
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Restriction fragment length polymorphisms in FVIII:C gene and their application in the linkage analysis of hemophilia A].
    He XP; Du CS; Zeng RP; An YH; Liu LL
    Yi Chuan Xue Bao; 1991; 18(5):394-400. PubMed ID: 1685886
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Molecular genetics of hemophilia A.
    Gitschier J
    Schweiz Med Wochenschr; 1989 Sep; 119(39):1329-31. PubMed ID: 2508218
    [TBL] [Abstract][Full Text] [Related]  

  • 38. High-resolution combined linkage physical map of short tandem repeat loci on human chromosome band Xq28 for indirect haemophilia A carrier detection.
    Machado FB; Medina-Acosta E
    Haemophilia; 2009 Jan; 15(1):297-308. PubMed ID: 18752533
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Screening of mutations of hemophilia A in 40 Italian patients: a novel G-to-A mutation in intron 10 of the F8 gene as a putative cause of mild hemophilia A in southern Italy.
    Santacroce R; Santoro R; Sessa F; Iannaccaro P; Sarno M; Longo V; Gallone A; Vecchione G; Muleo G; Margaglione M
    Blood Coagul Fibrinolysis; 2008 Apr; 19(3):197-202. PubMed ID: 18388498
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Application study on inversion diagnosis of F8 gene in hemophilia A].
    Qi LY; Jin CL; Lin CK; Ren MH; Dong WH; Sun KL
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Aug; 24(4):405-8. PubMed ID: 17680530
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 17.