DIAGNOSIS OF HAEMOPHILIA B CARRIERS USING INTRAGENIC OLIGONUCLEOTIDE PROBES
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference10 articles.
1. Carrier detection in haemophilia B using two further intragenic restriction fragment length polymorphisms;Winship;Nucl Acids Res,1984
2. Characterisation and use of an intragenic polymorphic marker for detection of carriers of haemophilia B (factor IX deficiency);Giannelli;Lancet,1984
3. A new MspI restriction fragment length polymorphism in the hemophilia B locus;Camerino;J Hum Genet,1985
4. Use of a BamHI polymorphism in the factor IX gene for the determination of hemophilia B carrier status;Hay;Blood,1986
5. The molecular genetics of haemophilia A and B;Brownlee;J Cell Sci,1986
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1. Direct carrier testing of haemophilia B by SSCP;Clinical & Laboratory Haematology;2008-06-28
2. Molekularbiologie und Genetik der Hämophilie B;Hämostaseologie;1999
3. Recurrent mutations in the factor IX gene: founder effect or repeat de novo events;Human Genetics;1993-08
4. An MseI RFLP in the 5’flanking region of the factor IX gene: its use for haemophilia B carrier detection in Caucasian and Thai populations;British Journal of Haematology;1993-05
5. The contribution of DNA analysis to carrier detection and prenatal diagnosis of hemophilia A and B;Annals of Hematology;1992-01
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