This cluster is characterized by the highest range of all morphological characteristics: average test size (range 336.82-383.19 [micro]m; average 357.33 [micro]m), mean proloculus size (range 11.89-16.73 [micro]m; average 15.19 [micro]m), number of chambers (range 9.57-10.64; average 10.23), and dextrality (range 54.54-76.19%; average 70.31%).
Differences between the sexes for associations between handedness and cerebral anatomy (Amunts, Jaencke, Mohlberg, Steimetz, & Zilles, 2000; Witelson, 1989) may be due to greater dextrality in some mixed-handed females.
Annett (1985) has suggested that the 'right shift' factor that promotes dextrality is more strongly expressed in females than in males, a feature that could account for the apparent fact seen in family handedness studies that left-handedness is slightly more common in males than in females.
Whereas Levy suggested that dextrality was favourable for spatial abilities and sinistrality favourable for verbal abilities, Annett's theory suggests (Annett, 1995, [ILLUSTRATION FOR FIGURE 3 OMITTED], p.
Individuals with two copies (rs + + homozygotes) show a weak left hand performance and a strong tendency to dextrality due to a substantial impairment of the right hemisphere.
For example, those with the least bias to dextrality seem to show the greatest ability in arithmetical (Annett & Manning, 1990a) and in spatial (Annett, 1992 b) skills.
Annett (1972) proposed that chance is the main determinant of handedness in all humans (and other primates) but that the chances are biased towards dextrality in most humans as a by-product of something which gives a left hemisphere advantage for speech.
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