Overview of Molecular Genetic Diagnosis
Author:
Affiliation:
1. University of Alabama at Birmingham Birmingham Alabama
Publisher
Wiley
Subject
General Medicine
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/0471142905.hg0901s76
Reference36 articles.
1. TRINUCLEOTIDE REPEAT EXPANSION AND HUMAN DISEASE
2. Int22h-related inversions causing hemophilia A: a novel insight into their origin and a new more discriminant PCR test for their detection
3. Linkage Analysis in the Next-Generation Sequencing Era
4. Detection of 98% of DMD/BMD gene deletions by polymerase chain reaction
Cited by 4 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. Molecular Genetics of Inherited Retinal Diseases;Inherited Retinal Disease;2022
2. An Overview of Molecular Genetic Diagnosis Techniques;Current Protocols in Human Genetics;2020-02-27
3. Point mutation in the TGFBI gene: surface-enhanced infrared absorption spectroscopy (SEIRAS) as an analytical method;Chemical Papers;2019-10-01
4. PCR-sequencing is a complementary method to amplification refractory mutation system for EGFR gene mutation analysis in FFPE samples;Experimental and Molecular Pathology;2015-12
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