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Thus, early in hominin evolution, an enhanced capacity to strike downward on an opponent may have given tall males a greater capacity to compete for mates and to defend their resources and offspring.
Compared with males, a greater number of areas had no female suicide data (B2).
Compared to males, a greater proportion of female patients was obese and had poorer glycemic control.
Similarly, in males a greater degree of slumped sitting posture was observed in the C2 cluster, but again the statistical evidence for this was only very weak.
It was hypothesized that a sex specific effect at eae 13 might be responsive to testosterone levels and, thereby, give males a greater ability to control disease once it is initiated.
Group 2 had a greater proportion of males, a greater proportion with siblings, multiple births, a mother who smokes, a mother who smoked during pregnancy, any smokers in the household, ≥2 smokers in the household, >5 individuals in the household, and, on average, the infants weighed more at birth (Table 1).
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Although the gender balance in this study reflects the ratio of asylum-seekers in Norway, where most are male, a greater number of girls in the follow-up may have enabled us to detect significant gender differences.
TG levels were 16.4%% higher in males versus females; males had a greater risk of hypertriglyceridemia (risk ratio 1.25; 95 % CI 1.24, 1.26; P < 0.0001).
IIIM males were more likely to mate than YM males, and a greater percent of IIIM males emerged after being held as pupae at 4, 16, or 28° for 3 d (Hamm et al. 2009).
Overall, polygynous males fledged more genetic offspring than monogamous males, but first-year polygynous males lost a greater share of within-pair paternity.
Ablated males turned more poorly than sham-ablated males, as determined by the percentage of males having a greater number of good turns versus poor turns, primarily because ablated males did more early turns.
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