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 *

203 related articles for article (PubMed ID: 2126393)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. [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]  

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

  • 6. 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]  

  • 7. 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]  

  • 8. [Possibilities of prenatal diagnosis in hemophilia A based on DNA analysis].
    Németi M; Bolodár A; Török O; Papp Z
    Orv Hetil; 1990 Jul; 131(30):1635-8. PubMed ID: 2119490
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. [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]  

  • 11. 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]  

  • 12. Carrier detection and prenatal diagnosis of hemophilia in developing countries.
    Peyvandi F
    Semin Thromb Hemost; 2005 Nov; 31(5):544-54. PubMed ID: 16276463
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. An improved method for prenatal diagnosis of genetic diseases by analysis of amplified DNA sequences. Application to hemophilia A.
    Kogan SC; Doherty M; Gitschier J
    N Engl J Med; 1987 Oct; 317(16):985-90. PubMed ID: 3657865
    [TBL] [Abstract][Full Text] [Related]  

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

  • 16. 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]  

  • 17. [Gene diagnosis of hemophilia A by PCR].
    Feng J
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1991 Oct; 13(5):384-8. PubMed ID: 1839260
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The use of DNA markers for carrier detection and prenatal diagnosis of haemophilia A in Egyptian families.
    Hussein IR; El-Beshlawy A; Salem A; Mosaad R; Zaghloul N; Ragab L; Fayek H; Gaber K; El-Ekiabi M
    Haemophilia; 2008 Sep; 14(5):1082-7. PubMed ID: 18547262
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [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]  

  • 20. 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]  

    [Next]    [New Search]
    of 11.