CONGENITAL FACTOR XIII DEFICIENCY: TYPE I AND TYPE II DISEASE
Open Access
- 1 June 1985
- journal article
- Published by Wiley in British Journal of Haematology
- Vol. 60 (2) , 375-376
- https://doi.org/10.1111/j.1365-2141.1985.tb07423.x
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- Hereditary factor XIII deficiency: report of four families and definition of the carrier stateBritish Journal of Haematology, 1984
- Factor XIII Levels in Five Families of Patients with Inherited Factor XIII Deficiency: Support for an Autosomal Recessive InheritanceThrombosis and Haemostasis, 1983
- Demonstration of a double hereditary pattern for congenital afibrinogenemiaAnnals of Hematology, 1981
- Factor XIII DeficiencyActa Haematologica, 1979
- Subunits A and S Inheritance in Four Families with Congenital Factor XIII DeficiencyBritish Journal of Haematology, 1978
- A Tentative Classification of Factor XIII Deficiency in Two GroupsActa Haematologica, 1977
- Immunological Studies of Coagulation Factor XIIIJournal of Clinical Investigation, 1973