Familial multiple coagulation factor deficiencies - chance associations and distinct clinical disorders
Author:
Publisher
Wiley
Subject
Genetics(clinical),Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2516.2008.01897.x/fullpdf
Reference69 articles.
1. Familial multiple coagulation factor deficiencies. I. Review of the literature: differentiation of single hereditary disorders associated with multiple factor deficiencies from coincidental concurrence of single factor deficiency states;Soff;Semin Thromb Hemost,1981
2. Familial multiple coagulation factor deficiencies. II. Combined factor VIII, IX, and XI deficiency and combined factor IX and XI deficiency: two previously uncharacterized familial multiple factor deficiency syndromes;Soff;Semin Thromb Hemost,1981
3. Congenital familial deficiency of factor V (parahaemophilia) combined with deficiency of antihaemophilic globulin;Iversen;Br J Haematol,1956
4. Combined deficiency of factor V and factor VIII (antihaemophilic globulin). A report of three cases;Jones;Br J Haematol,1962
5. Combined factor-V and factor-VIII deficiency: report of four cases;Seligsohn;Br J Haematol,1969
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