Renner W.,2000
Renner W., Koppel H., Brodmann M., Pabst E., Schallmoser K., Toplak H., Wascher T.C., Pilger E. Factor II G20210A and factor V G1691A gene mutations and peripheral arterial acclusive disease. - Thromb.Haemost., 2000, v. 83, p. 20-22.
Renner W., Koppel H., Brodmann M., Pabst E., Schallmoser K., Toplak H., Wascher T.C., Pilger E. Factor II G20210A and factor V G1691A gene mutations and peripheral arterial occlusive disease. - Thromb.Haemost., 2000, v. 83, p. 20-22.
