Download PDF
Thromb Haemost 1993; 70(02): 371
DOI: 10.1055/s-0038-1649583
Letter to the Editor
Schattauer GmbH Stuttgart

Factor VIII and IX Genes Polymorphisms in a Brazilian Black Population

Valder R Arruda
Department of Clinical Medicine, Hemocentro da Unicamp, School of Medical Science, State University of Campinas, CP-6198 CEP-13081, Campinas-SP-Brazil
,
Joyce M Annichino-Bizzachi
Department of Clinical Medicine, Hemocentro da Unicamp, School of Medical Science, State University of Campinas, CP-6198 CEP-13081, Campinas-SP-Brazil
,
Maria de Fatima Sonati
Department of Clinical Medicine, Hemocentro da Unicamp, School of Medical Science, State University of Campinas, CP-6198 CEP-13081, Campinas-SP-Brazil
,
Fernando F Costa
Department of Clinical Medicine, Hemocentro da Unicamp, School of Medical Science, State University of Campinas, CP-6198 CEP-13081, Campinas-SP-Brazil
› Author Affiliations
Further Information

Publication History

Received 29 October 1992

Accepted after revision 05 February 1993

Publication Date:
04 July 2018 (online)

  PDF Download  Permissions and Reprints
 

  • References

  • 1 Kogan SC, Doherty M, Gitschier J. An improved method for prenatal diagnosis of genetic diseases by analysis of amplified DNA sequences. Application to hemophilia A. N Engl J Med 1987; 317: 985-990
    CrossrefPubMedGoogle Scholar
  • 2 Graham JB, Kunkel GR, Fowlkes DM, Lord ST. The utility of a HindIII polymorphism of factor VIII examined by rapid DNA analysis. Br J Haematol 1990; 76: 75-79
    CrossrefPubMedGoogle Scholar
  • 3 Camerino G, Grzeschik KH, Jaye M, De La Salle H, Tolsloshev P, Lecoq JP, Heilig R, Mandel JL. Regional localisation on the human X chromosome and polymorphism of the coagulation factor IX gene (haemophilia B). Proc Natl Acad Sci USA 1984; 81: 498-501
    CrossrefPubMedGoogle Scholar
  • 4 Winship PR, Anson DS, Rizza CR, Brownlee GG. Carrier detection in haemophilia B using two further intragenic restriction fragment length polymorphisms. Nucl Acid Res 1989; 12: 8861-8872
    PubMedGoogle Scholar
  • 5 Peake I. Registry of DNA polymorphisms within or close to the human factor VIII and IX genes. Thromb Haemostas 1992; 67: 277-280
    PubMedGoogle Scholar
  • 6 Mercier B, Gaicher C, Mazuzier C. Detection of the TaqI polymorphism of the factor IX gene by PCR. Thromb Res 1991; 62: 599-601
    CrossrefPubMedGoogle Scholar
  • 7 Surin VL, Zhukova EL, Krutov AA, Solovyev GYa, Grineva NI. Simple and convenient detection of a HindIII polymorphic site in intron 19 of factor VIII gene using PCR. Nucl Acid Res 1990; 19: 3432
    PubMedGoogle Scholar
  • 8 Bowen DJ, Thomas P, Webb CE, Bignell P, Peake IR, Bloom AL. Facile and rapid analysis of three DNA polymorphisms within the human factor IX gene using the polymerase chain reaction. Br J Haematol 1991; 77: 559-560
    PubMedGoogle Scholar
  • 9 Zago MA, Costa FF. Hereditary haemoglobin disorders in Brazil. Trans R Soc Trop Med Hyg 1985; 79: 385-388
    CrossrefPubMedGoogle Scholar