Clinical Utility of SNP Microarray in Developmental Delay: A Rare Genetic Condition-Potocki-Lupski Syndrome (PTLS) From India-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Clinical Utility of SNP Microarray in Developmental Delay: A Rare Genetic Condition-Potocki-Lupski Syndrome (PTLS) From India

Published:2017-03-22 Issue:2 Volume:4 Page:
ISSN:2471-0016
Container-title:International Clinical Pathology Journal
language:
Short-container-title:ICPJL

Author:

Dave Usha P

Publisher

MedCrave Group, LLC

Reference10 articles.

1. 2) and delineation of a dosage-sensitive critical interval that can convey an autism phenotype;Potocki;Am J Hum Genet,2007

2. 2);Treadwell-Deering;J Dev Behav Pediatr,2010

3. Searching for Potocki-Lupski syndrome phenotype: A patient with language impairment and no autism;Gulhan Ercan-Sencicek;Brain Dev,2012

4. A new chemical diagnostic method for inborn errors of metabolism by mass spectrometry-rapid, practical and simultaneous urinary metabolites analysis;Matsumoto;Mass Spectrometry Reviews,1996

5. Sanchez-Valle A, Pierpont ME, Potocki L. The severe end of the spectrum: hypoplastic left heart in Potocki-Lupski syndrome. Am J Med Genet A. 2011;155A(2):363–366.

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