BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

668 related articles for article (PubMed ID: 2907834)

  • 1. [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]  

  • 2. [Genetic diagnosis in haemophiliacs (haemophilia A, B, carrier)].
    Mikami S
    Rinsho Byori; 1990 Jun; Suppl 85():102-13. PubMed ID: 1976834
    [No Abstract]   [Full Text] [Related]  

  • 3. Molecular basis of hemophilia.
    Lozier JN; High KA
    Hematol Pathol; 1990; 4(1):1-26. PubMed ID: 2111315
    [No Abstract]   [Full Text] [Related]  

  • 4. The use of deoxyribonucleic acid probes in the evaluation of hemophilia.
    Howard PL
    Ann Clin Lab Sci; 1987; 17(1):8-13. PubMed ID: 2883925
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Molecular diagnosis in patients and carriers of hemophilia A and B].
    Mantilla-Capacho J; Beltrán-Miranda CP; Jaloma-Cruz AR
    Gac Med Mex; 2005; 141(1):69-71. PubMed ID: 15754755
    [No Abstract]   [Full Text] [Related]  

  • 6. [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]  

  • 7. Molecular biology of the hemophilias.
    Thompson AR
    Prog Hemost Thromb; 1991; 10():175-214. PubMed ID: 1901173
    [No Abstract]   [Full Text] [Related]  

  • 8. DNA polymorphisms for carrier detection of hemophilia in Thailand.
    Chuansumrit A; Goodeve A; Sasanakul W; Peake IR; Pintadit P; Hathirat P; Preston FE; Isarangkul P
    Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():201-6. PubMed ID: 8629107
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Genetic factors in hemophilia].
    Rozynkowa D
    Acta Haematol Pol; 1987; 18(1-2):96-100. PubMed ID: 3124485
    [No Abstract]   [Full Text] [Related]  

  • 10. 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]  

  • 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. From hemophilia B to hemophilia A via the fragile X locus: genes and recombination in the distal region of the human X chromosome long arm.
    Oberlé I; Mandel JL
    Horiz Biochem Biophys; 1986; 8():51-89. PubMed ID: 2875934
    [No Abstract]   [Full Text] [Related]  

  • 13. 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]  

  • 14. A factor IX gene probe: its use in carrier detection, antenatal diagnosis and characterisation of the molecular basis for hemophilia B.
    Trent RJ; Svirklys L; Power PA; Rickard KA; Lammi A; Kronenberg H
    Aust N Z J Med; 1985 Dec; 15(6):721-6. PubMed ID: 3869438
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Detection of carrier status of hemophilia B using DNA markers.
    Ishak R; Zakaria Z
    Southeast Asian J Trop Med Public Health; 1997 Sep; 28(3):629-30. PubMed ID: 9561621
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Intragenic polymorphisms of factor VIII and IX genes and their utility in the indirect diagnosis of carriers of Haemophilias A and B].
    Borjas L; Zabala W; Pineda L; Pardo T; Fernández E; Zambrano M; Quintero JM; Arteaga-Vizcaíno M; Morales-Machín A; Delgado W
    Invest Clin; 2010 Sep; 51(3):391-401. PubMed ID: 21305775
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Absence of correlation between X chromosome inactivation pattern and plasma concentration of factor VIII and factor IX in carriers of haemophilia A and B.
    Orstavik KH; Scheibel E; Ingerslev J; Schwartz M
    Thromb Haemost; 2000 Mar; 83(3):433-7. PubMed ID: 10744150
    [TBL] [Abstract][Full Text] [Related]  

  • 18. RFLPs of factor IX gene in Japanese haemophilia B families and gene deletion in two high-responder-inhibitor patients.
    Mikami S; Nishino M; Nishimura T; Fukui H
    Jinrui Idengaku Zasshi; 1987 Mar; 32(1):21-31. PubMed ID: 2886685
    [No Abstract]   [Full Text] [Related]  

  • 19. [Molecular analysis and genetic diagnosis of hemophilia. b. Hemophilia B].
    Kojima T
    Nihon Rinsho; 1987 Dec; 45(12):2941-6. PubMed ID: 2895820
    [No Abstract]   [Full Text] [Related]  

  • 20. Molecular genetics and counselling in haemophilia.
    Peake I
    Thromb Haemost; 1995 Jul; 74(1):40-4. PubMed ID: 8578494
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 34.