Characterization of a Rare Single α-Globin Gene Deletion in a Chinese Woman with Hb H Disease
Author:
Publisher
Informa UK Limited
Subject
Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.1080/03630260500312618
Reference4 articles.
1. A rapid and reliable 7-deletion multiplex polymerase chain reaction assay for α-thalassemia
2. A novel α-thalassemia-2 (−2.7-kb) observed in a chinese patient with Hb H disease
3. Mutation nomenclature extensions and suggestions to describe complex mutations: A discussion
Cited by 10 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 spectrum of α‐ and β‐thalassemia among individuals of reproductive age in the Zhuhai region of southern China;International Journal of Laboratory Hematology;2023-03-14
2. Investigation of the mechanism of copy number variations involving the α-globin gene cluster on chromosome 16: two case reports and literature review;Molecular Genetics and Genomics;2022-11-03
3. The value of single-molecule real-time technology in the diagnosis of rare thalassemia variants and analysis of phenotype–genotype correlation;Journal of Human Genetics;2021-10-25
4. Identification of Three Types of α-Thalassemia Deletion, –α21.9, –α2.4, and – –THAI, and Their Frequencies, in One Family in the Population of Southern Guangxi Zhuang Autonomous Region, People’s Republic of China;Hemoglobin;2018-01-02
5. Identification of the −α2.4Deletion in One Family and in One Hb H Disease Patient in Guangxi, People’s Republic of China;Hemoglobin;2016-03-17
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