Facile and rapid analysis of three DNA polymorphisms within the human factor IX gene using the polymerase chain reaction
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.1991.tb08626.x/fullpdf
Reference7 articles.
1. Regional localisation on the human X chromosome and polymorphism of the coagulation factor IX gene (haemophilia B locus);Camerino;Proceedings of the National Academy of Sciences of the United States of America,1984
2. Characterisation and use of an intragenic polymorphic marker for detection of carriers of haemophilia B (factor IX deficiency);Giannelli;Lancet,1984
3. The Malmo polymorphism of factor IX: establishing the genotypes by rapid analysis of DNA;Graham;Blood,1989
4. Prenatal diagnosis of haemostatic disorders;Mibashan;Methods in Haematology,1989
5. Carrier detection in haemophilia B using two further intragenic restriction fragment length polymorphisms;Winship;Nucleic Acids Research,1984
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2. Prenatal diagnosis of haemophilia B: the Italian experience;Haemophilia;2013-06-28
3. Direct carrier testing of haemophilia B by SSCP;Clinical & Laboratory Haematology;2008-06-28
4. A common G10430A mutation (Gly 60 Ser) in the factor IX gene describes the presence of moderate and mild hemophilia B in the majority of the Gujarati population;Annals of Hematology;2007-02-17
5. The molecular analysis of haemophilia B: a guideline from the UK haemophilia centre doctors' organization haemophilia genetics laboratory network;Haemophilia;2005-07
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