Rapid screening of 10 common mutations in Turkish Gaucher patients using electronic DNA microarray
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Hematology,Molecular Biology,Molecular Medicine
Reference8 articles.
1. Microelectronic array system for molecular diagnostic genotyping: Nanogen NanoChip® 400 and Molecular Biology Workstation;Keen-Kim;Expert Rev. Mol. Diagn.,2006
2. Active microelectronic array system for DNA hybridization, genotyping and pharmacogenomic applications;Sosnowski;Psychiatr. Genet.,2002
3. Gaucher disease: multiple lessons from a single gene disorder;Beutler;Acta Pædiatr., Suppl.,2006
4. Detection of the defect of Gaucher's disease and its carrier state in peripheral-blood leukocytes;Beutler;Lancet,1970
5. Analysis of three mutations in Turkish children with Gaucher disease;Gurakan;J. Inherit. Metab. Dis.,1999
Cited by 7 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. Clinical-genetic characteristics and treatment outcomes of Turkish children with Gaucher disease type 1 and type 3: A sixteen year single-center experience;European Journal of Medical Genetics;2021-11
2. Inborn Errors of Metabolism;Advances in Clinical Chemistry;2016
3. Evaluation of SNPs in the Mitochondrial DNA Using NanoChip Microarrays in the Turkish Population;International Journal of Human Genetics;2015-09
4. Recent advances in the molecular diagnosis of inborn errors of metabolism;Clinical Biochemistry;2014-06
5. Rapid Molecular Diagnosis of Genetic Diseases by High Resolution Melting Analysis: Fabry and Glycogen Storage 1A Diseases;Genetic Testing and Molecular Biomarkers;2014-01
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