| Literature DB >> 21810622 |
R M Cruz1, J K Hartsfield, G Falcão-Alencar, D L Koller, R W Pereira, J Mah, I Ferrari, S F Oliveira.
Abstract
The role played by genetic components in the etiology of the Class III phenotype, a class of dental malocclusion, is not yet understood. Regions that may be related to the development of Class III malocclusion have been suggested previously. The aim of this study was to search for genetic linkage with 6 microsatellite markers (D1S234, D4S3038, D6S1689, D7S503, D10S1483, and D19S566), near previously proposed candidate regions for Class III. We performed a two-point parametric linkage analysis for 42 affected individuals from 10 Brazilian families with a positive Class III malocclusion segregation. Analysis of our data indicated that there was no evidence for linkage of any of the 6 microsatellite markers to a Class III locus at = zero, with data supporting exclusion for 5 of the 6 markers evaluated. The present work reinforces that Class III is likely to demonstrate locus heterogeneity, and there is a dependency of the genetic background of the population in linkage studies.Mesh：
Year: 2011 PMID： 21810622 PMCID： PMC6761732 DOI： 10.1177/0022034511416668
Source DB: PubMed Journal: J Dent Res ISSN： 0022-0345 Impact factor: 6.116