F8 and F9 mutations fail to co-segregate in a family with co-incident haemophilia A and B
Author:
Publisher
Wiley
Subject
Genetics(clinical),Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2516.2010.02396.x/fullpdf
Reference17 articles.
1. Familial multiple coagulation factor deficiencies - chance associations and distinct clinical disorders;Robson;Haemophilia,2009
2. The rare coagulation disorders--review with guidelines for management from the United Kingdom Haemophilia Centre Doctors’ Organisation;Bolton-Maggs;Haemophilia,2004
3. Management of von Willebrand disease: a guideline from the UK Haemophilia Centre Doctors’ Organization;Pasi;Haemophilia,2004
4. Combined clotting factor deficiencies: experience at a single hemophilia treatment center;O’Brien;Haemophilia,2007
5. The effect of combined factor XI deficiency with von Willebrand factor abnormalities on haemorrhagic diathesis;Tavori;Thromb Haemost,1990
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