1. Acquila M, Pasino M, Lanza T, Bottini F, Molinari AC, Bicocchi MP (2004) Duplication of exon 13 causes one third of the cases of mild hemophilia A in northern Italy. Haematologica 89:758–759
2. Bagnall RD, Waseem N, Green PM, Gianelli F (2002) Recurrent inversion breaking intron 1 of the factor VIII gene is a frequent cause of severe hemophilia A. Blood 99:168–174
3. D’Andrea G, Colaizzo D, Vecchione G, Grandone E, Di Minno G, Margaglione M (2002) GLAnzmann’s Thrombasthenia Italian Team (GLATIT). Glanzmann’s thrombasthenia: identification of 19 new mutations in 30 patients. Thromb Haemost 87:1034–1042
4. Deszo D, Ventura C, Moreira I, DinizMJ, Antunes M, Tavares A, Araùjo F, MoraisS, Campos M, Lavina J, Kemball-Cook J (2006) The spectrum of mutations and molecular pathogenesis of hemophilia A in 181 Portuguese patients. Haematologica 91:840–843
5. Fernández-López O, García-Lozano J-R, Núñez-Vázquez R, Pérez-Garrido R, Núñez-Roldán A (2005) The spectrum of mutations in Southern Spanish patients with hemophilia A and identification of 28 novel mutations. Haematologica 90:707–710