BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

225 related articles for article (PubMed ID: 2896074)

  • 1. [Study on Bcl I RFLP in factor VIII gene and prenatal diagnosis of hemophilia A through RFLP].
    Shen Y; Wu GY; Wang SW; Gao QS; Xin X; Sun NH; Wang FY; Wu YZ; Ning Y; Long GF
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1987 Dec; 9(6):402-6. PubMed ID: 2896074
    [No Abstract]   [Full Text] [Related]  

  • 2. [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]  

  • 3. First experiences in application of RFLP analysis for carrier detection in preparation of prenatal diagnosis of hemophilia A in the GDR.
    Herrmann FH; Kruse T; Wehnert M; Vogel G; Wulff K
    Folia Haematol Int Mag Klin Morphol Blutforsch; 1988; 115(4):489-93. PubMed ID: 2465959
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Rapid genotyping of XbaI and MspI DNA polymorphisms of the human factor VIII gene: estimation of their combined heterozygosity in the Argentinean population.
    De Brasi CD; Rossetti LC; Larripa IB
    Haematologica; 2003 Feb; 88(2):232-4. PubMed ID: 12604420
    [No Abstract]   [Full Text] [Related]  

  • 5. [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]  

  • 6. [Carrier detection and prenatal diagnosis for hemophilia A using the inversion analysis of the factor VIII gene].
    Okamoto Y; Kojima T; Katsumi A; Yamazaki T; Hamaguchi M; Nishida M; Suzumori K; Saito H
    Rinsho Ketsueki; 1995 Nov; 36(11):1252-6. PubMed ID: 8691564
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Inversion mutation as a major cause of severe hemophilia A in Italian patients.
    Mori PG; Caprino D; Bicocchi MP; Valetto A; Bottini F; Aquila M
    Haematologica; 1997; 82(1):75-6. PubMed ID: 9107090
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Prenatal diagnosis in hemophilia A using factor VIII gene polymorphism--Indian experience.
    Chowdhury MR; Tiwari M; Kabra M; Menon PS
    Ann Hematol; 2003 Jul; 82(7):427-30. PubMed ID: 12768323
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Prenatal diagnosis of hemophilia involving grandpaternal mosaicism.
    Lebo RV; Koerper MA; Kim JH; Chueh J; Golbus MS
    Am J Med Genet; 1993 Sep; 47(3):401-4. PubMed ID: 7907841
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Carrier detection and prenatal diagnosis in haemophilia A and B.
    Chistolini A; Papacchini M; Mazzucconi MG; La Verde G; Arcieri R; Ferrari A; Paesano R; Pachi A; Mariani G
    Haematologica; 1990; 75(5):424-8. PubMed ID: 1982946
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. [Gene mutation and gene diagnosis of hemophilia].
    Kojima T
    Nihon Seirigaku Zasshi; 1998; 60(1):31-42. PubMed ID: 9614303
    [No Abstract]   [Full Text] [Related]  

  • 13. 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]  

  • 14. [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]  

  • 15. [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]  

  • 16. 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]  

  • 17. Amplification of Bcl I region of the factor VIII gene by PCR.
    Ishak R; Khim LC
    Southeast Asian J Trop Med Public Health; 1996 Jun; 27(2):364-6. PubMed ID: 9280004
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Utility of an exon 14 BslI polymorphism for improved genetic diagnosis of hemophilia A in Indian population.
    Mukundan P; Shetty S; Kulkarni B; Ghosh K
    Prenat Diagn; 2008 Oct; 28(10):920-2. PubMed ID: 18702107
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Structure and function of factor VIII and factor IX gene and molecular DNA diagnosis in hemophilia A and B].
    Herrmann FH; Wehnert M; Wulff K
    Z Arztl Fortbild (Jena); 1988; 82(22):1116-22. PubMed ID: 2907834
    [No Abstract]   [Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 12.