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Genetic markers in Welsh gypsies.

机译:威尔士吉普赛人的遗传标记。

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摘要

Data are presented on polymorphic genetic markers of 84 Welsh gypsies, members of an inbred population characterised by a high incidence of phenylketonuria and other recessively inherited diseases. Sixteen polymorphic loci were studied: the ABO blood group distribution was comparable to that of the surrounding population, the B gene frequency being 7-5%, a lower frequency than most earlier studies in gypsies. The haptoglobin 1 gene frequency (23-7%) was very different from that of the British population, resembling the frequency found in India and some previously reported gypsy groups. The data on Welsh gypsies for the various loci are discussed in relation to the known evidence for a number of European gypsy populations, and in relation to the genetic structure of these populations. It is concluded that genetic divergence has occurred in the European gypsies, and that this may have been accentuated by the dispersal, isolation, and inbreeding which have occurred during the present century.
机译:数据提供了84个威尔士吉普赛人的多态遗传标记,这是近交人群的特征,其特征为苯丙酮尿症和其他隐性遗传疾病的发生率很高。研究了16个多态位点:ABO血型分布与周围人群相当,B基因频率为7-5%,比大多数吉普赛人早期研究的频率低。触珠蛋白1基因的频率(23-7%)与英国人群的频率非常不同,类似于印度和一些先前报道的吉普赛族的频率。讨论了有关多个基因座的威尔士吉普赛人的数据,并与许多欧洲吉普赛人的已知证据以及这些人的遗传结构进行了讨论。可以得出结论,欧洲吉普赛人已经发生了遗传分歧,并且本世纪以来发生的传播,隔离和近交可能加剧了这种分歧。

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