Paternal uniparental disomy of chromosome 15 in a child with angelman syndrome
Author:
Publisher
Wiley
Subject
Clinical Neurology,Neurology
Reference43 articles.
1. Clayton-Smith J Am J Med Genet 1992
2. Zori RT Hendrickson J Woolven S J Pediatr Neurol 1992
3. The association of Angelman's syndrome with deletions within 15q11-q13;Pembrey;J Med Genet,1989
4. Incidence of 15q deletions in the Angelman syndrome: a survey of twelve affected persons;Williams;Am J Med Genet,1989
5. Comparison of the 15q deletions in Prader-Willi and Angelman syndromes: specific regions, extent of deletions, parental origin, and clinical consequences;Magenis;Am J Med Genet,1990
Cited by 58 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. Non-pathological complete paternal uniparental isodisomy of chromosome 2 revealed in a maternity testing case;International Journal of Legal Medicine;2018-05-25
2. Confined placental mosaicism and its impact on confirmation of NIPT results;American Journal of Medical Genetics Part C: Seminars in Medical Genetics;2016-05-17
3. Angelman syndrome caused by deletion: A genotype–phenotype correlation determined by breakpoint;Epilepsy Research;2013-07
4. Epilepsy in Korean patients with Angelman syndrome;Korean Journal of Pediatrics;2012
5. New mechanisms involved in paternal 20q disomy associated with pseudohypoparathyroidism;European Journal of Endocrinology;2010-12
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