1. Abildgaard CF, Harrison J (1974) Fletcher factor deficiency: Family study and détection. Blood 43: 641–644
2. Aghai E, Yaniv I, David M (1984) Factor XI deficiency in an Arab Moslem family in Israel. Scand J Haematol 32: 327–331
3. Aguercif M, Anner R, Ritchard J, Nydegger U, Soria J, Bouvier CA (1972) Syndromes de dysfibrino-génémie congénitales et familiales. A propos de deux nouvelles familles. Pediatrie 27: 317–323
4. Alexander B, Goldstein R, Landwehr G, Cook CD, Addelson E, Wilson C (1952) Congenital SPCA deficiency. A hitherto unrecognized coagulation defect with hemorrhage rectified by sérum and sérum fractions. J Clin Invest 30: 596–608
5. Alexandre P, Larcan A, Briquel ME (1980) Recurring thrombo-embolic accidents caused by family-related deficiency of the fibrinolysis system. Blut 41: 437–444