Increasing evidence that germline mutations inCHEK2do not cause Li-Fraumeni syndrome
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference10 articles.
1. Mutation analysis of the CHK2 gene in families with hereditary breast cancer;Allinen;Br J Cancer,2001
2. Heterozygous germ line hCHK2 mutations in Li-Fraumeni syndrome;Bell;Science,1999
3. Li-Fraumeni syndrome;Birch;Eur J Cancer,1994
4. Prevalence and diversity of constitutional mutations in the p53 gene among 21 Li-Fraumeni families;Birch;Cancer Res,1994
5. Detection of 11 germline inactivating p53 mutations and absence of TP63 and HCHK2 mutations in 17 French families with Li-Fraumeni or Li-Fraumeni like syndrome;Bougeard;J Med Genet,2001
Cited by 47 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. Implementation of a dyadic nomenclature for monogenic diseases;The American Journal of Human Genetics;2024-09
2. Synergistic Antitumor Activity of Talazoparib and Temozolomide in Malignant Rhabdoid Tumors;Cancers;2024-05-28
3. Management of individuals with germline pathogenic/likely pathogenic variants in CHEK2: A clinical practice resource of the American College of Medical Genetics and Genomics (ACMG);Genetics in Medicine;2023-10
4. CHEK2is not a Li-Fraumeni syndrome gene: time to update public resources;Journal of Medical Genetics;2023-08-03
5. Germline mutations in the PALB2 and CHEK2 genes and hereditary cancer;Ural Medical Journal;2023-06-30
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