Mosaic maternal uniparental disomy of chromosome 15 in Prader-Willi syndrome: Utility of genome-wide SNP array

Author:

Izumi Kosuke,Santani Avni B.,Deardorff Matthew A.,Feret Holly A.,Tischler Tanya,Thiel Brian D.,Mulchandani Surabhi,Stolle Catherine A.,Spinner Nancy B.,Zackai Elaine H.,Conlin Laura K.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference20 articles.

1. A rapid microarray based whole genome analysis for detection of uniparental disomy;Altug-Teber;Hum Mutat,2005

2. Trisomy 15 with loss of the paternal 15 as a cause of Prader-Willi syndrome due to maternal disomy;Cassidy;Am J Hum Genet,1992

3. Prader-Willi syndrome;Cassidy;Genet Med,2012

4. Conlin LK Kaur M Izumi K Close L Wilkens A Clarks D Dearderff MA Zackai EH Pallisrer P Hakonarson H Spinner NB Krantz ID Utility of SNP Arrays in Detecting, Quantifying, and Determining Meiotic Origin of Tetrasomy 12p in Blood from Individuals with Pallister-Killian Syndrome

5. Mechanisms of mosaicism, chimerism and uniparental disomy identified by single nucleotide polymorphism array analysis;Conlin;Hum Mol Genet,2010

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

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