Mutations in the thrombomodulin and endothelial protein C receptor genes in women with late fetal loss
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2141.2001.02964.x/fullpdf
Reference35 articles.
1. Thrombophilic polymorphisms are common in women with fetal loss without apparent cause;Brenner;Thrombosis and Haemostasis,1999
2. The short loop between epidermal growth factor-like domains 4 and 5 is critical for human thrombomodulin function;Clarke;Journal of Biological Chemistry,1993
3. The importance of primary diagnosis in perinatal death;Davies;American Journal of Obstetric and Gynecology,1985
4. Structure and function of thrombomodulin: a natural anticoagulant;Dittman;Blood,1990
5. A mutation in the thrombomodulin gene, 127G to A coding for Ala25Thr, and the risk of myocardial infarction in men;Doggen;Thrombosis and Haemostasis,1998
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