One hundred and seventy-eight (87.3%), twenty (9.8%), and five (2.5%) of them were classified as basic type, simulated divergence excess type, and true divergence excess type intermittent exotropia, respectively, according to the Burian classification [ 9].
The exodrift in intermittent exotropia of basic type, simulated divergence excess type, and true divergence excess type was similar at 6 weeks (4.6 ± 7.5, 2.85 ± 12.5, and −1.2 ± 3.90, resp., P = 0.082 Kruskal Wallis test) and at 3 years postoperatively (7.8 ± 8.20, 8.2 ± 11.75, and 1.6 ± 3.0, resp., P = 0.078 Kruskal Wallis test).
We validated this basic expectation of divergence with gene flow and then used the resultant heterogeneity in genomic divergence to characterize the shape and depth of the species boundary as a function of divergent selection, phylogenetic distance, and hybridization.
The normal form method (NFM) presented in Part I [1] is applied to the analysis of systems near two basic bifurcation conditions: divergence and flutter.
For more information on some basic concepts of divergence measures, we refer the reader to, for example, [2 5] and references therein.
The medical records of 180 consecutive patients who had undergone RR or ULR for basic or pseudo-divergence excess-type intermittent exotropia of 20 to 25 PD by one surgeon (D.G.C).
In this article, we studied two basic types of functional divergence (type-I and type-II) in depth in order to give an accurate estimation of functional divergence-related sites.
The separation of adjacent lamellae and its decrease at higher strain rate are consistent with pressure from molecular cilia emerging from fold surfaces, in a similar way to the basic cause of lamellar divergence in spherulites.
However, beyond such basic agreements, there is divergence in thought and actions, particularly as it relates to the religious pluralism.
