Detection of imprinting mutations in Angelman syndrome using a probe for exon α ofSNRPN-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Detection of imprinting mutations in Angelman syndrome using a probe for exon α ofSNRPN

Published:1996-05-17 Issue:2 Volume:63 Page:414-415
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Beuten Joke,Sutcliffe James S.,Casey Brett M.,Beaudet Arthur L.,Hennekam Raoul C. M.,Willems Patrick J.

Publisher

Wiley

Subject

Genetics (clinical)

Reference15 articles.

1. Angelman syndrome in an inbred family

2. Inherited microdeletions in the Angelman and Prader–Willi syndromes define an imprinting centre on human chromosome 15

3. Clinical research on Angelman syndrome in the United Kingdom: Observations on 82 affected individuals

4. Molecular diagnosis of the Prader-Willi and Angelman syndromes by detection of parent-of-origin specific DNA methylation in 15q11-13

5. Modification of 15q11 — q13 DNA methylation imprints in unique Angelman and Prader — Willi patients

Cited by 11 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. Developmental Delay: Gene Testing;Molecular Pathology in Clinical Practice;2016

2. Epigenomic strategies at the interface of genetic and environmental risk factors for autism;Journal of Human Genetics;2013-05-16

3. Developmental Disabilities;Molecular Pathology in Clinical Practice: Genetics;2009

4. Developmental Disabilities;Molecular Pathology in Clinical Practice;2007

5. Prenatal diagnosis of a homologous Robertsonian translocation involving chromosome 15;Prenatal Diagnosis;2001

同舟云学术

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