Genotype-phenotype correlations among TP53 carriers: Literature review and analysis of probands undergoing multi-gene panel testing and single-gene testing
Author:
Funder
Australian National Health and Medical Research
Publisher
Elsevier BV
Subject
Cancer Research,Genetics,Molecular Biology
Reference25 articles.
1. Rhabdomyosarcoma in children: epidemiologic study and identification of a familial cancer syndrome;Li;J Natl Cancer Inst,1969
2. Revisiting Li-fraumeni syndrome from TP53 mutation carriers;Bougeard;J Clin Oncol,2015
3. NCCN guidelines insights: genetic/familial high-risk assessment: breast and ovarian, version 2.2017;Daly;J Natl Compr Canc Netw,2017
4. The 2016 Li-fraumeni syndrome cancer spectrum;Caron;J Clin Oncol,2016
5. Cancer screening recommendations for individuals with Li-fraumeni syndrome;Kratz;Clin Cancer Res,2017
Cited by 11 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. Germline p.R181H variant in TP53 in a family exemplifying the genotype-phenotype correlations in Li-Fraumeni syndrome;Familial Cancer;2024-09-11
2. Functional evaluation of germline TP53 variants identified in Brazilian families at-risk for Li–Fraumeni syndrome;Scientific Reports;2024-07-26
3. Current prospects of hereditary adrenal tumors: towards better clinical management;Hereditary Cancer in Clinical Practice;2024-03-26
4. Clinical and Genetic Analysis of Li-Fraumeni Syndrome with Novel TP53 Mutations;2024-01-03
5. Clinical Classification and Molecular Interpretation of Hereditary Cancer Patients with Germline Pathogenic Tp53 Variations;2024
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