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For age it turned out to be difficult to find sufficient studies with comparable selections of age categories to run meta-analysis on, therefore in the results a qualitative summation is given for all relevant age data found.
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For analyses of extra-Poisson variation between years, it was not possible to take account of year-on-year variations in population size because of a lack of data for the relevant age range within the study area over the full study period.
No clear patterns of increased or decreased risk for any particular age (data not shown) or biologically relevant periods in life (Table 3) were observed for endometrial cancer.
Therefore, prevalence data were taken from different sources and adjusted to the relevant age categories.
We do agree that our fit for the younger age groups is not as good as our excellent fits for the older – and more relevant – age groups and this finding might be due to a lack of relevant biological data for these age groups.
Data on lifetime exposures are often self-reported in epidemiologic studies, sometimes many years after the relevant age.
To determine data-relevant age cohorts, we tested young mice at 3-4 months-of-age, middle-aged mice at 10-12 months-of-age, and old mice at 18-24 months-of-age.
We found no relevant age-dependent differences.
Season with aged data.
Relevant data included age and clinical classification of acne.
Patient's relevant sociodemographic data included age, gender, current smoking (more than one cigarette daily), and history of alcohol consumption.
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