Barnes DG and Dourson ML (1988). Reference dose (RfD): Description and use in health risk assessment. Regul. Toxicol. Pharmacol. 8: 471-486.
2.
Calabrese EJ (1985). Uncertainty factors and interindividual variation. Regul. Toxicol. Pharmacol. 5: 190-196.
3.
Dourson ML, Felter SP, and Robinson D. (1996). Evolution of science-based uncertainty factors in noncancer risk assessment. Regul. Toxicol. Pharmacol. 24: 108-120.
4.
Dourson ML and Stara JF (1983). Regulatory history and experimental support of uncertainty (safety) factors. Regul. Toxicol. Pharmacol. 3: 238-244.
5.
Environmental Protection Agency (1998). Framework for refining FQPA science policies, Staff paper #12. Washington, D.C.
6.
Hattis D., Erdeich L., and Ballew M. (1987). Human variability and susceptibility to toxic chemicals. Risk Anal. 7: 415-426.
7.
House Commerce Committee ( 1996). Food quality protection act of 1996. 104th Congress, 2nd session. Report 104-669. Washington, D.C., p. 43.
8.
National Academy of Science ( 1987). Regulating Pesticides in Food: The Delaney Paradox. National Academy Press, Washington, D.C.
9.
National Academy of Science ( 1993). Pesticides in the Diets of Infants and Children. National Academy Press, Washington, D.C.
10.
Renwick AG (1998). Toxicokinetics in infants and children in relation to the ADI and TDI. Food Addit. Contam. 15: 17-35.
11.
Renwick AG and Lazarus NR (1998). Human variability and noncancer risk assessment-An analysis of the default uncertainty fac; tor. Regul. Toxicol. Pharmacol. 27: 3-20.
