Roma (Gypsies): Genetic Studies
Author:
Publisher
Wiley
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/9780470015902.a0006239.pub3
Reference71 articles.
1. Null Mutations in LTBP2 Cause Primary Congenital Glaucoma
2. High prevalence of theW24X mutation in the gene encoding connexin-26 (GJB2) in Spanish Romani (gypsies) with autosomal recessive non-syndromic hearing loss
3. Cystic fibrosis mutations and associated haplotypes in Bulgaria - a comparative population genetic study
4. Challenges of diagnostic exome sequencing in an inbred founder population
5. LTBP2 and CYP1B1 mutations and associated ocular phenotypes in the Roma/Gypsy founder population
Cited by 5 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Admixture Has Shaped Romani Genetic Diversity in Clinically Relevant Variants;Frontiers in Genetics;2021-06-16
2. Hearing impairment locus heterogeneity and identification of PLS1 as a new autosomal dominant gene in Hungarian Roma;European Journal of Human Genetics;2019-03-14
3. Origins, admixture and founder lineages in European Roma;European Journal of Human Genetics;2015-09-16
4. Clinical Applications and Implications of Common and Founder Mutations in Indian Subpopulations;Human Mutation;2014-11-27
5. The Outsiders: Power Differentials between Roma and Non-Roma in Europe;Perspectives on European Politics and Society;2014-01-02
1.学者识别学者识别
2.学术分析学术分析
3.人才评估人才评估
"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370
www.globalauthorid.com
TOP
Copyright © 2019-2024 北京同舟云网络信息技术有限公司 京公网安备11010802033243号 京ICP备18003416号-3