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References in periodicals archive ?
The difference between the breast cancer risk perception level of the participants and the 5-year breast cancer risk level calculated according to the Gail Model was significant (p<0.01).
The 5-year breast cancer risk level of 7.1% of the participants was found to be over 1.67% according to the Gail Model (Table 1).
What is the breast cancer risk levels perceived in midwives and nurses?
Given priors based on the national on-site average weighted by the house's dilution estimates, the mean cancer risk level at the time of the initial sale was 1.23 X [10.sup.-5], and the mean change between updated risk levels and prior risk levels was -7.80 X [10.sup.-6].
[FIGURE 1 OMITTED] Table 1 Descriptive Statistics for the Sample of Repeat Sale Houses Variable Mean Standard Deviation Price at time of initial sale ($) 70,520 22,938 Change in price between repeat 7172 6774 sales ($) Cancer risk level at time of 12.30 38.60 initial sale X 1 million (prior = national average) Change in cancer risk level between -7.80 28.52 repeat sales X 1 million (prior = national average) Cancer risk level at time of 4.93 22.30 initial sale X 1 million (prior = state average) Change in cancer risk level -2.60 13.92 between repeat sales X 1 million (prior = state average) Dummy variable indicating if house 0.31 0.46 was sold after the EPA's Remedial Investigation for the closest site (0/1) Change in Remedial Investigation 0.63 0.48 for the closest site (0/1) No.
We do not assume that people know the site-specific risks before the release of the EPA's studies providing estimates of the cancer risk levels. Rather, we make the more realistic assumption that people base their estimates of site risks on their general knowledge of Superfund sites.
Similarly, biomarker concentrations approached or exceeded concentrations consistent with cancer risk levels > 1 x [10.sup.-6] for a number of analytes.
The results presented here indicate that, even at the GM biomarker concentrations, cancer risk levels are > 1 x [10.sup.-6] for several analytes, and, for some analytes, > 1 x [10.sup.-3].
The variable results are due in part to differences in patients" cancer risk levels, differences in the patient preparation procedures used across studies, and differences in the types of technology used, the task force found.
For those chemicals classified as either known or probable human carcinogens, 21 of the agencies reported using specific excess lifetime cancer risk levels to develop standards or guidelines.
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