A new genomic mechanism leading to cri-du-chat syndrome
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference18 articles.
1. Monosomy 1p36 breakpoint junctions suggest pre-meiotic breakage-fusion-bridge cycles are involved in generating terminal deletions
2. Prenatal detection of ade novo terminal inverted duplication 4p in a fetus with the Wolf-Hirschhorn syndrome phenotype
3. Inverted duplications are recurrent rearrangements always associated with a distal deletion: description of a new case involving 2q
4. Modulation of Non-Templated Nucleotide Addition by Taq DNA Polymerase: Primer Modifications that Facilitate Genotyping
5. . 2004. Chromosome Abnormalities and Genetic Counseling. , , , , , editors. New York: Oxford University Press. 577 p.
Cited by 16 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. FISH Diagnostics of Chromosomal Translocation with the Technology of Synthesis of Locus-Specific DNA Probes Based on Long-Range PCR;Russian Journal of Genetics;2020-06
2. A de novo Chromosomal Abnormality in Cri du Chat Syndrome;The Indian Journal of Pediatrics;2013-07-31
3. The Role of ATM in the Deficiency in Nonhomologous End-Joining near Telomeres in a Human Cancer Cell Line;PLoS Genetics;2013-03-28
4. Mechanisms of telomere loss and their consequences for chromosome instability;Frontiers in Oncology;2012
5. Chromosomal Structural Rearrangements: Detection and Elucidation of Mechanisms Using Cytogenomic Technologies;Clinics in Laboratory Medicine;2011-12
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