Genetic Studies of Prader-Willi Patients Provide Evidence for Conservation of Genomic Architecture in Proximal Chromosome 15q-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Genetic Studies of Prader-Willi Patients Provide Evidence for Conservation of Genomic Architecture in Proximal Chromosome 15q

Published:2010-12 Issue: Volume: Page:no-no
ISSN:0003-4800
Container-title:Annals of Human Genetics
language:en
Short-container-title:

Author:

Hou Aihua,Lin Shuan-Pei,Ho Shi Yun,Chen Chi-Fung Jennifer,Lin Hsiang-Yu,Chen Yen-Juin,Huang Chi-Yu,Chiu Huei-Ching,Chuang Chih-Kuang,Chen Ken-Shiung

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1469-1809.2010.00633.x/fullpdf

Reference54 articles.

1. Genomic microarrays in human genetic disease and cancer;Albertson;Hum Mol Genet,2003

2. Chromosome breakage in the Prader-Willi and Angelman syndromes involves recombination between large, transcribed repeats at proximal and distal breakpoints;Amos-Landgraf;Am J Hum Genet,1999

3. Microarray analysis of gene/transcript expression in Prader-Willi syndrome: Deletion versus UPD;Bittel;J Med Genet,2003

4. The phenotypic manifestations of interstitial duplications of proximal 15q with special reference to the autistic spectrum disorders;Bolton;Am J Med Genet,2001

5. Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome: Implications for imprint-switch models, genetic counseling, and prenatal diagnosis;Buiting;Am J Hum Genet,1998

Cited by 1 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. Uniparental Disomy of Chromosome 15 in Two Cases by Chromosome Microarray: A Lesson Worth Thinking;Cytogenetic and Genome Research;2017

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