4 The Hemophilias

This publication has 100 references indexed in Scilit:

• Severe Hemophilia A in a Female by Cryptic Translocation: Order and Orientation of Factor VIII within Xq28
  Genomics, 1993
• Evidence that descendants of three founders constitute about 25% of hemophilia B in the united states
  Genomics, 1991
• Genetics and molecular biology of haemophilias A and B
  Blood Coagulation & Fibrinolysis, 1991
• Detection of three novel mutations in two haemophilia A patients by rapid screening of whole essential region of factor VIII gene
  The Lancet, 1991
• Human factor IXLincoln Park: a molecular characterization
  Molecular and Cellular Probes, 1990
• A past mutation at Isoleucine³⁹⁷ is now a common cause of moderate/mild haemophilia B
  British Journal of Haematology, 1990
• DETECTION OF POLYMORPHISMS AT CYTOSINE PHOSPHOGUANADINE DINUCLEOTIDES AND DIAGNOSIS OF HAEMOPHILIA B CARRIERS
  The Lancet, 1989
• Gene for human factor X: a blood coagulation factor whose gene organization is essentially identical with that of factor IX and protein C
  Biochemistry, 1986
• Hemophilia A
  New England Journal of Medicine, 1985
• Haemophilia B caused by a point mutation in a donor splice junction of the human factor IX gene
  Nature, 1985