DHPLC screening of cystic fibrosis gene mutations
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference34 articles.
1. Diagnostic Testing for Rett Syndrome by DHPLC and Direct Sequencing Analysis of the MECP2 Gene: Identification of Several Novel Mutations and Polymorphisms
2. Analysis of the CFTR gene confirms the high genetic heterogeneity of the Spanish population: 43 mutations account for only 78% of CF chromosomes
3. Superiority of Denaturing High Performance Liquid Chromatography over single-stranded conformation and conformation-sensitive gel electrophoresis for mutation detection in TSC2
4. The Cystic Fibrosis Gene: Isolation and Significance
5. Using CCM and DHPLC to detect mutations in the glucocorticoid receptor in atherosclerosis: a comparison
Cited by 38 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. Can paranasal sinus computed tomography (CT) screen for cystic fibrosis heterozygotes?;Panminerva Medica;2019-02
2. Exophiala dermatitidis Revealing Cystic Fibrosis in Adult Patients with Chronic Pulmonary Disease;Mycopathologia;2017-11-01
3. Genotoxicity Detection at the Molecular Level in Food Safety Assessment: Conventional Methods and Developments;Functional Nucleic Acids Detection in Food Safety;2016
4. Discordant diagnoses obtained by different approaches in antithrombin mutation analysis;Clinical Biochemistry;2014-09
5. Novel and rareCFTRgene mutations in Turkish patients with congenital aplasia of vas deferens;Andrologia;2012-12-12
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