The prevalence of chromosome 22q11.2 deletions in 2,478 children with cardiovascular malformations. A population-based study
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference53 articles.
1. Children diagnosed with congenital cardiac malformations at the national university departments of pediatric cardiology: Positive predictive values of data in the Danish National Patient Registry;Agergaard;Clin Epidemiol,2011a
2. Can clinical assessment detect 22q11.2 deletions in patients with cardiac malformations? A review;Agergaard;Eur J Med Genet,2011b
3. 22q11 deletions in isolated and syndromic patients with tetralogy of Fallot;Amati;Hum Genet,1995
4. Conotruncal heart defects: Impact of genetic syndromes on immediate operative mortality;Anaclerio;Ital Heart J,2004
5. The Danish National Hospital Register. A valuable source of data for modern health sciences;Andersen;Dan Med Bull,1999
Cited by 36 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. In-Depth Genomic Analysis: The New Challenge in Congenital Heart Disease;International Journal of Molecular Sciences;2024-02-01
2. Genetics of Common Birth Defects in Newborns;Principles of Neonatology;2024
3. Decoding 22q11.2: prenatal profiling and first‐trimester risk assessment in Danish nationwide cohort;Ultrasound in Obstetrics & Gynecology;2024-01
4. Coarctation of the Aorta: Modern Paradigms Across the Lifespan;Hypertension;2023-10
5. Genetic Basis of Congenital Heart Disease;Clinical and Surgical Aspects of Congenital Heart Diseases;2023
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