Molecular Updating of β-Thalassemia Mutations in the Upper Egyptian Population
Author:
Publisher
Informa UK Limited
Subject
Biochemistry, medical,Clinical Biochemistry,Genetics(clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.3109/03630269.2010.526440
Reference36 articles.
1. Improvements in the HbVar database of human hemoglobin variants and thalassemia mutations for population and sequence variation studies
2. Keynote Address: The Challenge of Thalassemia for the Developing Countries
3. Identification of Mediterranean β-Thalassemia Mutations by Reverse DOT-Blot in Italians and Egyptians
4. Identification of novel Asian Indian and Japanese mutations causing β-thalassaemia in the Egyptian population
Cited by 17 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. The Spectrum of Beta-Thalassemia Mutations in Syrian Refugees and Turkish Citizens;Cureus;2021-06-04
2. Molecular characterization of β-thalassemia intermedia in the West Bank, Palestine;BMC Hematology;2019-02-18
3. Impact of Genotype of Beta Globin Gene on Hepatic and Myocardial Iron Content in Egyptian Patients with Beta Thalassemia;Indian Journal of Hematology and Blood Transfusion;2018-11-08
4. Molecular characterization of exonic rearrangements and frame shifts in the dystrophin gene in Duchenne muscular dystrophy patients in a Saudi community;Human Genomics;2018-04-10
5. Analysis of Common β-Thalassemia Mutations in North Vietnam;Hemoglobin;2018-01-02
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