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 *

374 related articles for article (PubMed ID: 2575737)

  • 1. 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]  

  • 2. Hemophilia A carrier detection by restriction fragment length polymorphism analysis and discriminant analysis based on ELISA of factor VIII and vWf.
    Poon MC; Hoar DI; Low S; Pon JK; Anand S; Sinclair GD
    J Lab Clin Med; 1992 Jun; 119(6):751-62. PubMed ID: 1350611
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. Carrier detection and prenatal diagnosis in families with haemophilia.
    Shetty S; Ghosh K; Bhide A; Mohanty D
    Natl Med J India; 2001; 14(2):81-3. PubMed ID: 11396323
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Carrier detection of haemophilia B by using an intragenic restriction-fragment length polymorphism.
    Bröcker-Vriends AH; Briët E; Quadt R; Bertina RM; van der Linden IK; van de Kamp JJ; Pearson PL; Veltkamp JJ
    Thromb Haemost; 1985 Aug; 54(2):506-9. PubMed ID: 3001965
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Recombinant DNA methods in hemophilia A: carrier detection and prenatal diagnosis.
    Sadler JE
    Semin Thromb Hemost; 1990 Oct; 16(4):341-7. PubMed ID: 2126393
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genomic diagnosis of haemophilia A and B in the German Democratic Republic.
    Herrmann FH; Wehnert M; Schröder W
    Folia Haematol Int Mag Klin Morphol Blutforsch; 1990; 117(4):601-7. PubMed ID: 1714866
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [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]  

  • 14. Carrier detection of Hemophilia B by using a restriction site polymorphism associated with the coagulation Factor IX gene.
    Grunebaum L; Cazenave JP; Camerino G; Kloepfer C; Mandel JL; Tolstoshev P; Jaye M; De la Salle H; Lecocq JP
    J Clin Invest; 1984 May; 73(5):1491-5. PubMed ID: 6325506
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. [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]  

  • 18. Extragenic factor IX gene RFLP is useful for detecting carriers of Japanese hemophilia B.
    Tanimoto M; Kojima T; Ogata K; Hamaguchi M; Takamatsu J; Kamiya T; Saito H
    Nihon Ketsueki Gakkai Zasshi; 1989 Jul; 52(4):774-7. PubMed ID: 2575831
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 19.