Hb Q-Thailand-Hb H disease in a chinese living in Geneva, Switzerland: Characterization of the variant and identification of the two α-thalassemic chromosomes
Author:
Publisher
Wiley
Subject
Hematology
Reference21 articles.
1. Splenectomy in Two Cases of Haemoglobin Q-H-Disease (Hb Q-α-Thalassaemia)
2. Further Cases of Hb Q-H Disease (Hb Q-α Thalassemia)
3. The alpha-globin gene adjacent to the gene for HbQ-alpha 74 Asp replaced by His is deleted, but not that adjacent to the gene for HbG- alpha 30 Glu replaced by Gln; three-fourths of the alpha-globin genes are deleted in HbQ-alpha-thalassemia
4. The Genetic Basis of Hb Q-H Disease
Cited by 13 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. Hemoglobin profile and molecular characteristics of the complex interaction of hemoglobin Doi-Saket [α9(A7) asn > lys, HBA2:c.30C > a], a novel α2α1 hybrid globin variant, with hemoglobin E [β26(B8) Glu > lys, HBB:c.79G > A] and deletional α + -thalassemia in a Thai family;Annals of Medicine;2023-10-05
2. Hemoglobin Q-Thailand and its Combinations with other Forms of Thalassemia or Hemoglobinopathies in Northern Thailand;Clinical Laboratory;2014
3. Prevalence and molecular characterization of abnormal hemoglobin in eastern Guangdong of southern China;Clinical Genetics;2011-01-31
4. Hemoglobin Q-Thailand related disorders: Origin, molecular, hematological and diagnostic aspects;Blood Cells, Molecules, and Diseases;2010-10
5. Complex interaction of Hb Q-Thailand and Hb E with α0-thalassemia and hereditary persistence of fetal hemoglobin in a Chinese family;Annals of Hematology;2010-03-24
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