1. Aledort, L. M. (1982). Current concepts in diagnosis and management of hemophilia. Hospital Practice (Office Ed.), 17, 77–84. 89–92.
2. Bagnall, R. D., Waseem, N., Green, P. M., et al. (2002). Recurrent inversion breaking intron 1 of the factor VIII gene is a frequent cause of severe hemophilia A. Blood, 99, 168–174.
3. Becker, J., Schwaab, R., Moller Taube, A., et al. (1996). Characterization of the factor VIII defect in 147 patients with sporadic hemophilia A: Family studies indicate a mutation type-dependent sex ratio of mutation frequencies. American Journal of Human Genetics, 58, 657–670.
4. Bhattacharyya, M. S., Singh, J., Soni, P., et al. (2003). Recombinant factor VIII for haemophilia. An overview of production technologies. CRIPS, 4, 2–8.
5. Brower, C., & Thompson, A. R. (2008). Hemophilia A. GeneReviews. Updated 25 Mar 2008. http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=hemo-a