Factor VIII and IX Genes Polymorphisms in a Brazilian Black Population

• 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
• 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
• 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
• 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
• 5 Peake I. Registry of DNA polymorphisms within or close to the human factor VIII and IX genes. Thromb Haemostas 1992; 67: 277-280
• 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
• 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
• 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
• 9 Zago MA, Costa FF. Hereditary haemoglobin disorders in Brazil. Trans R Soc Trop Med Hyg 1985; 79: 385-388