Carrier detection and feasibility of prenatal diagnosis of hemophilia B by multiplex polymerase chain reaction

This publication has 10 references indexed in Scilit:

• Carrier detection for hemophilia B: Evaluation of multiple polymorphic sites
  American Journal of Hematology, 1990
• 3 Factor IX
  Bailliere's Clinical Haematology, 1989
• DETECTION OF POLYMORPHISMS AT CYTOSINE PHOSPHOGUANADINE DINUCLEOTIDES AND DIAGNOSIS OF HAEMOPHILIA B CARRIERS
  The Lancet, 1989
• Direct detection of point mutations by mismatch analysis: application to haemophilia B
  Nucleic Acids Research, 1989
• Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase
  Science, 1988
• Use of a BamHI polymorphism in the factor IX gene for the determination of hemophilia B carrier status
  Blood, 1986
• A new MspI restriction fragment length polymorphism in the hemophilia B locus
  Human Genetics, 1985
• Complete nucleotide sequences of the gene for human factor IX (antihemophilic factor B)
  Biochemistry, 1985
• Carrier detection in haemophilia B using two further intragenic restriction fragment length polymorphisms
  Nucleic Acids Research, 1984
• Regional localization on the human X chromosome and polymorphism of the coagulation factor IX gene (hemophilia B locus).
  Proceedings of the National Academy of Sciences, 1984