The genetics of congenital heart disease: a review of recent developments
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Cardiology and Cardiovascular Medicine
Reference46 articles.
1. Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome
2. Diversity and Functional Consequences of Germline and Somatic PTPN11 Mutations in Human Disease
3. PTPN11 (Shp2) Mutations in LEOPARD Syndrome Have Dominant Negative, Not Activating, Effects
4. Germline mutations in HRAS proto-oncogene cause Costello syndrome
5. HRAS mutations in Costello syndrome: Detection of constitutional activating mutations in codon 12 and 13 and loss of wild-type allele in malignancy
Cited by 56 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. Understanding the Genetic and Non-Genetic Interconnections in the Aetiology of Syndromic Congenital Heart Disease: An Updated Review: Part 2;Current Cardiology Reports;2024-02-15
2. Cardiovascular embryology and foetal heart development;Genomic and Molecular Cardiovascular Medicine;2024
3. Tissue specific trisomy 15 mosaicism associated with urogenital malformations;European Journal of Medical Genetics;2023-10
4. Environmental changes surrounding congenital heart disease;Clinical and Experimental Pediatrics;2023-08-15
5. Identification of long non-coding RNA in formaldehyde-induced cardiac dysplasia in rats;Food and Chemical Toxicology;2023-04
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