Collaboratively charting the gene-to-phenotype network of human congenital heart defects-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Collaboratively charting the gene-to-phenotype network of human congenital heart defects

Published:2010 Issue:3 Volume:2 Page:16
ISSN:1756-994X
Container-title:Genome Medicine
language:en
Short-container-title:Genome Medicine

Author:

Barriot Roland,Breckpot Jeroen,Thienpont Bernard,Brohée Sylvain,Van Vooren Steven,Coessens Bert,Tranchevent Leon-Charles,Van Loo Peter,Gewillig Marc,Devriendt Koenraad,Moreau Yves

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics,Molecular Biology,Molecular Medicine

Cited by 24 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. SORBS2 is a genetic factor contributing to cardiac malformation of 4q deletion syndrome patients;eLife;2021-06-08

2. SORBS2 is a genetic factor contributing to cardiac malformation of 4q deletion syndrome;2020-05-14

3. Technologies to Study Genetics and Molecular Pathways;Congenital Heart Diseases: The Broken Heart;2016

4. Novel Loci for Non-Syndromic Coarctation of the Aorta in Sporadic and Familial Cases;PLOS ONE;2015-05-18

5. The diagnostic value of next generation sequencing in familial nonsyndromic congenital heart defects;American Journal of Medical Genetics Part A;2015-04-30

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