BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

209 related articles for article (PubMed ID: 11798076)

  • 21. 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]  

  • 22. Direct and indirect gene diagnosis of hemophilia A pedigrees in the Chinese population.
    Cao Y; Shen L; Huang R; Yang L; Du Z; Ma H; Zheng T; Gu H; Li H
    Mol Med Rep; 2017 Oct; 16(4):5722-5728. PubMed ID: 28849064
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [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]  

  • 24. Prevalence of the factor 8 gene intron 1 inversion in Chinese haemophiliacs and its application to carrier detection and prenatal diagnosis in haemophilia A families.
    Lu YL; Wang XF; Ding QL; Dai J; Xi XD; Wang HL
    Haemophilia; 2011 May; 17(3):541-2. PubMed ID: 21118339
    [No Abstract]   [Full Text] [Related]  

  • 25. [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]  

  • 26. Screening of intron 1 inversion and three intragenic factor VIII gene polymorphisms in Pakistani hemophilia A families.
    Bugvi SM; Imran M; Mahmood S; Hafeez R; Fatima W; Sohail S
    Blood Coagul Fibrinolysis; 2012 Mar; 23(2):132-7. PubMed ID: 22270795
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Use of Intron 1 and 22 inversions and linkage analysis in carrier detection of hemophilia A in Indians.
    Ahmed R; Kannan M; Biswas A; Ranjan R; Choudhry VP; Saxena R
    Clin Chim Acta; 2006 Mar; 365(1-2):109-12. PubMed ID: 16129422
    [TBL] [Abstract][Full Text] [Related]  

  • 29. The prevalence study on restriction fragment length polymorphism analysis for the detection of hemophilia A carrier.
    Song KS; Lee CH; Chung CS; Lee K; Yang YH; Kim KY
    Yonsei Med J; 1993 Sep; 34(3):239-42. PubMed ID: 7903130
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Application studies on the gene diagnosis and carrier detection of hemophilia A by using polymerase chain reaction-conformation sensitive gel electrophoresis].
    Lillicrap D; He GP; Leggo J; Liu YS; Tong XH; Zhou GX; Luo LH
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Aug; 26(4):393-9. PubMed ID: 20017302
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Genomic carrier detection and prenatal diagnosis of haemophilia A in families at risk using the polymerase chain reaction (PCR).
    Wehnert M; Shukova EL; Surin VL; Schröder W; Solovjev GYa ; Grinjeva NI; Herrmann FH
    Folia Haematol Int Mag Klin Morphol Blutforsch; 1990; 117(4):617-22. PubMed ID: 1714868
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [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]  

  • 33. Hemophilia A. Detection of molecular defects and of carriers by DNA analysis.
    Antonarakis SE; Waber PG; Kittur SD; Patel AS; Kazazian HH; Mellis MA; Counts RB; Stamatoyannopoulos G; Bowie EJ; Fass DN
    N Engl J Med; 1985 Oct; 313(14):842-8. PubMed ID: 2993888
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Introns 1 and 22 inversions and F8 gene sequencing for molecular diagnosis of hemophilia A in Chile].
    Poggi H; Honorato J; Romeo E; Zúñiga P; Quiroga T; Lagos M
    Rev Med Chil; 2011 Feb; 139(2):189-96. PubMed ID: 21773656
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Multiplex analysis of two intragenic microsatellite repeat polymorphisms in the genetic diagnosis of haemophilia A.
    Windsor S; Taylor SA; Lillicrap D
    Br J Haematol; 1994 Apr; 86(4):810-5. PubMed ID: 7918077
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. Combined use of DNA probes in first-trimester prenatal diagnosis of hemophilia A.
    Sampietro M; Camerino G; Romano M; Cappellini MD; Fiorelli G; Brambati B; Guerneri S; Ferrari M; Travi M; Krachmalnicoff A
    Thromb Haemost; 1987 Dec; 58(4):988-92. PubMed ID: 3127923
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Application of STR genetic marker system in the detection of hemophilia A carriers in Guangxi, China].
    Zhou JL; Wei HY; Wu H; Hu YL; Liang WL
    Zhongguo Dang Dai Er Ke Za Zhi; 2012 Dec; 14(12):951-5. PubMed ID: 23234785
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Factor VIII gene polymorphisms in the Asian Indian population.
    Chowdhury MR; Herrmann FH; Schroder W; Lambert CT; Lalloz MR; Layton M; Kumbnani HK; Kabra M; Menon PS; Verma IC
    Haemophilia; 2000 Nov; 6(6):625-30. PubMed ID: 11122386
    [TBL] [Abstract][Full Text] [Related]  

  • 40. The status of carrier and prenatal diagnosis of haemophilia in China.
    Dai J; Lu Y; Ding Q; Wang H; Xi X; Wang X
    Haemophilia; 2012 Mar; 18(2):235-40. PubMed ID: 21910785
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.