Author:
WESTON B. W.,MONAHAN P. E.
Subject
Genetics(clinical),Hematology,General Medicine
Reference33 articles.
1. Congenital combined deficiency of coagulation factors II, VII, IX, and X - report of a case;McMillan;N Engl J Med,1966
2. Congenital deficiency of blood clotting factors II, VII, IX, and X;Chung;Blood,1979
3. Combined deficiency of factors II, VII, IX and X (Borgschulte-Grigsby deficiency) in pregnancy;McMahon;Obstet Gynecol,2001
4. Combined deficiency of coagulation factors II, VII, IX, and X: a case of probable congenital origin;Ekelund;Pediatr Hematol Oncol,1986
5. Founder mutation Arg485Pro led to recurrent compound heterozygous GGCX genotypes in two German patients with VCCFD type 1;Rost;Blood Coagul Fibrinolysis,2006
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