References
- Casson, P.R., Krawetz, S.A., Diamond, M.P., Zhang, H., Legro, R.S., Schlaff, W.D., (2011) Proactively Establishing a Biologic Specimens Repository for Large Clinical Trials: An Idea Whose Time has Come. Syst Biol Reprod Med 57:217–221.
- Krawetz, S.A., Casson, P.R., Diamond, M.P., Zhang, H., Legro, R.S., Schlaff, W.D., (2011 ) Establishing a Biologic Specimens Reprository for Reproductive Clinical Trails: Technical Aspects. Syst Biol Reprod Med 57:222–227.
- Levy, D., Splansky, G., Strand, N., Atwood, L., Benjamin, E., Blease, S., (2010) Consent for genetic research in the Framingham Heart Study. Am J Med Genet A 152A:1250–1256.
- McQuillan, G., Porter, K., Agelli, M., Kington, R. (2003) Consent for genetic research in a general population: the NHANES experience. Genet Med. 5:35–42.
- Menikoff, J. (2010) The paradoxical problem with multiple-IRB reviews. New Engl J Med 363:1591–1593.
- Schlaff., W.D., Zhang., H., Diamond, M.P., Coutifaris, C., Casson, P.R., Brzyski, R.G., (2011) Increasing burden of institutional review in multicenter clinical trials of infertility: the Reproductive Medicine Network experience with the Pregnancy in Polycystic Ovary Syndrome (PPCOS) I and II studies. Fertil Steril 96:15–18