Testing for heritable thrombophilia in children at Starship Children's Hospital: An audit of requests between 2004 and 2009
Author:
Publisher
Wiley
Subject
Pediatrics, Perinatology, and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1440-1754.2012.02517.x/fullpdf
Reference18 articles.
1. Inherited antithrombin deficiency causing thrombophilia;Egeberg;Thromb. Diath. Haemorrh.,1965
2. Deficiency of protein C in congenital thrombotic disease;Griffin;J. Clin. Invest.,1981
3. Familial protein S deficiency is associated with recurrent thrombosis;Comp;J. Clin. Invest.,1984
4. Mutation in blood coagulation factor V associated with resistance to activated protein C;Bertina;Nature,1994
5. A common genetic variation in the 3′-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis;Poort;Blood,1996
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