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Genetic variation at twentythree microsatellite loci in sixteen human populations

dc.creatorDeka, Ranjan
dc.creatorShriver, Mark D.
dc.creatorYu, Ling Mei
dc.creatorMueller Heidreich, Elisa
dc.creatorJin, Li
dc.creatorZhong, Yixi
dc.creatorMcGarvey, Stephen T.
dc.creatorSwarup Agarwal, Shyam
dc.creatorBunker, Clareann H.
dc.creatorMiki, Tetsuro
dc.creatorHundrieser, Joachim
dc.creatorYin, Shih-Jiun
dc.creatorRaskin, Salmo
dc.creatorBarrantes Mesén, Ramiro
dc.creatorFerrell, Robert E.
dc.creatorChakraborty, Ranajit
dc.date.accessioned2015-05-26T22:02:33Z
dc.date.available2015-05-26T22:02:33Z
dc.date.issued1999-08
dc.descriptionArtículo científico -- Universidad de Costa Rica, Instituto de Investigaciones en Salud. 1999es_ES
dc.description.abstractWe have analysed genetic variation at 23 microsatellite loci in a global sample of 16 ethnically and geographically diverse human populations. On the basis of their ancestral heritage and geographic locations, the studied populations can be divided into five major groups, viz. African, Caucasian, Asian Mongoloid, American Indian and Pacific Islander. With respect to the distribution of alleles at the 23 loci, large variability exists among the examined populations. However, with the exception of the American Indians and the Pacific Islanders, populations within a continental group show a greater degree of similarity. Phylogenetic analyses based on allele frequencies at the examined loci show that the first split of the present-day human populations had occurred between the Africans and all of the non-African populations, lending support to an African origin of modern human populations. Gene diversity analyses show that the coefficient of gene diversity estimated from the 23 loci is, in general, larger for populations that have remained isolated and probably of smaller effective sizes, such as the American Indians and the Pacific Islanders. These analyses also demonstrate that the component of total gene diversity, which is attributed to variation between groups of populations, is significantly larger than that among populations within each group. The empirical data presented in this work and their analyses reaffirm that evolutionary histories and the extent of genetic variation among human populations can be studied using microsatellite loci.es_ES
dc.description.procedenceUCR::Vicerrectoría de Investigación::Unidades de Investigación::Ciencias de la Salud::Instituto de Investigaciones en Salud (INISA)es_ES
dc.description.sponsorshipUniversidad de Costa Rica. Instituto de Investigaciones en Saludes_ES
dc.identifier.citationhttp://link.springer.com/article/10.1007/BF02924561
dc.identifier.citationhttp://www.biomedcentral.com/1471-2156/9/86
dc.identifier.doi10.1007/BF02924561
dc.identifier.issn0022-1333
dc.identifier.issn0973-7731
dc.identifier.urihttps://hdl.handle.net/10669/13348
dc.language.isoen_USes_ES
dc.rightsacceso abierto
dc.sourceJournal of Genetics 78(2): 99-121es_ES
dc.subjectgenetic variationes_ES
dc.subjectgene diversityes_ES
dc.subjectGenética humanaes_ES
dc.subjectHuman geneticses_ES
dc.titleGenetic variation at twentythree microsatellite loci in sixteen human populationses_ES
dc.typeartículo original

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