<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Wang, B.</style></author><author><style face="normal" font="default" size="100%">Xia, Y.</style></author><author><style face="normal" font="default" size="100%">Song, J.</style></author><author><style face="normal" font="default" size="100%">Wang, W.</style></author><author><style face="normal" font="default" size="100%">Tang, Y.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Case Report: Potential Speciation in Humans Involving Robertsonian Translocations.</style></title><secondary-title><style face="normal" font="default" size="100%">Biomedical Research</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Chromosome</style></keyword><keyword><style  face="normal" font="default" size="100%">Evolution</style></keyword><keyword><style  face="normal" font="default" size="100%">Robertsonian translocation homozygosity</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2013</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://www.biomedres.info/biomedical-research/case-report-potential-speciation-in-humans-involving-robertsoniantranslocations.pdf</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">24</style></volume><pages><style face="normal" font="default" size="100%">171-174</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Approximately one person in 1,000 is a Robertsonian translocation carrier. This type of translocation most likely arises during egg (or more rarely sperm) formation. Most Robertsonian translocation carriers are healthy and have a normal lifespan, but do have an increased risk of pregnancy loss and children with trisomies. We have found a Robertsonian translocation family, one of them who came from a consanguinous marriage has the previously undescribed balanced human karyotype 44,XY,der(14;15)(q10;q10), der(14;15)(q10;q10). Many such rearrangements in natural populations of different species are known. It is well-known that the fitness of rob translocation carries is reduced, but rob translocation can provide material for evolution.&amp;nbsp;&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><section><style face="normal" font="default" size="100%">171</style></section></record></records></xml>