Inheritance of deficiency of fibrin-stabilizing factor (factor 13).
- 1 January 1970
- journal article
- Vol. 22 (1) , 89-95
Abstract
No abstract availableThis publication has 17 references indexed in Scilit:
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- New families with hereditary hemorrhagic trait due to deficiency of fibrin stabilizing factor (F. 13).1968
- The transpeptidase system which crosslinks fibrin by γ-glutamyl-ε-lysine bondsBiochemical and Biophysical Research Communications, 1968
- Amine specificity in transpeptidation. Inhibition of fibrin cross-linkingBiochemistry, 1968
- Factor XIII deficiency: Concentrations inrelatives of patients and in normal infantsThe Journal of Pediatrics, 1968
- INHERITANCE OF FIBRIN-STABILISING-FACTOR DEFICIENCYThe Lancet, 1968
- Congenital deficiency of factor XIII (fibrin-stabilizing factor)The American Journal of Medicine, 1967
- Factor 13 Deficiency with Severe Hemorrhagic DiathesisBlood, 1966
- [Study of a case of congenital deficiency of factor 13 (FSF)].1965
- A Case of Fibrin-Stabilizing Factor (FSF) DeficiencyThrombosis and Haemostasis, 1965