Clinical utility gene card for: familial erythrocytosis
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Link
http://www.nature.com/articles/ejhg2011252.pdf
Reference17 articles.
1. McMullin MF : Idiopathic erythrocytosis: a disappearing entity. Hematology Am Soc Hematol Educ Program 2009; 1: 629–635.
2. Percy MJ, Rumi E : Genetic origins and clinical phenotype of familial and acquired erythrocytosis and thrombocytosis. Am J Hematol 2009; 84: 46–54.
3. Gordeuk VR, Stockton DW, Prchal JT : Congenital polycythemias/erythrocytoses. Haematologica 2005; 90: 109–116.
4. Rives S, Pahl HL, Florensa L et al: Molecular genetic analyses in familial and sporadic congenital primary erythrocytosis. Haematologica 2007; 92: 674–677.
5. Ang SO, Chen H, Gordeuk VR et al: Endemic polycythemia in Russia: mutation in the VHL gene. Blood Cells Mol Dis 2002; 28: 57–62.
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. Erythrocytosis: genes and pathways involved in disease development;BLOOD TRANSFUS-ITALY;2021
2. The Participation of the Intrinsically Disordered Regions of the bHLH-PAS Transcription Factors in Disease Development;International Journal of Molecular Sciences;2021-03-11
3. First Description of Hb San Diego (HBB: c.328G>A) in a Chinese Family with Congenital Erythrocytosis;Hemoglobin;2019-03-04
4. Genetic variants of erythropoietin (EPO) and EPO receptor genes in familial erythrocytosis;International Journal of Laboratory Hematology;2018-12-03
5. Gene panel sequencing improves the diagnostic work-up of patients with idiopathic erythrocytosis and identifies new mutations;Haematologica;2016-09-20
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