Poort S.R.,1993
Poort S.R., Pabinger-Fasching I., Mannhalter C., Reitsma P.H., Bertina R.M. Twelve novel and two recurrent mutations in 14 Austrian families with hereditary protein C deficiency. - Blood Coagul.Fibrinolysis, 1993, v. 4, p. 4273-280.
Смотрите также:
