Lessons learned from a child with a chromosomal abnormality but no major congenital anomalies-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Lessons learned from a child with a chromosomal abnormality but no major congenital anomalies

Published:2020-07-28 Issue:3 Volume:26 Page:139-140
ISSN:1205-7088
Container-title:Paediatrics & Child Health
language:en
Short-container-title:

Author:

Zhou Shijie¹,Colaiacovo Samantha²,Djolovic Andrea³,Saleh Maha²³

Affiliation:

1. Schulich School of Medicine and Dentistry, Western University, London, Ontario

2. Division of Medical Genetics, Department of Paediatrics, London Health Sciences Centre, Western University, London, Ontario

3. Windsor Genetics Out-Reach Program of London Health Sciences, Windsor, Ontario

Publisher

Oxford University Press (OUP)

Subject

Pediatrics, Perinatology and Child Health

Link

http://academic.oup.com/pch/article-pdf/26/3/139/37410184/pxaa080.pdf

Reference6 articles.

1. Karyotype–phenotype analysis and molecular delineation of a 3p26 deletion/8q24.3 duplication case with a virtually normal phenotype and mild cognitive deficit;Shrimpton;Am J Med Genet A,2006

2. Duplication 9p and their implication to phenotype;Guilherme;BMC Med Genet,2014

3. A terminal 3p26.3 deletion is not associated with dysmorphic features and intellectual disability in a four-generation family;Moghadasi;Am J Med Genet A,2014

4. Array-CGH study of partial trisomy 9p without mental retardation;Bouhjar;Am J Med Genet A,2011

5. Genetic counselling difficulties and ethical implications of incidental findings from array-CGH: a 7-year national survey;Lefebvre;Clin Genet,2016

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