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A novel deletion causing alpha thalassemia clarifies the importance of the major human alpha globin regulatory element.

机译：引起α地中海贫血的新型缺失阐明了主要的人类α珠蛋白调节元件的重要性。

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Viprakasit V; Harteveld CL; Ayyub H; Stanley JS; Giordano PC; Wood WG; Higgs DR;
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年度 2006
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正文语种 eng
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1. A Severe Case of Hemoglobin H Disease due to Compound Heterozygosity for Deletion of the Major alpha-Globin Regulatory Element (MCS-R2) and alpha(0)-Thalassemia [J] . Huang Lv-Yin, Yan Jin-Mei, Zhou Jian-Ying, Acta Haematologica . 2017 ,第1期

机译：由于复方杂合性，缺失主要α-珠蛋白调控元素（MCS-R2）和α（0） - αSemia，严重的血红蛋白H病
2. A novel selective deletion of the major alpha-globin regulatory element (MCS-R2) causing alpha-thalassaemia [J] . Wu Man-Yu, He Yi, Yan Jin-Mei, British Journal of Haematology . 2017 ,第6期

机译：一种新颖的α-珠蛋白调节元素（MCS-R2）的新选择性缺失，导致α-地中海血症
3. Novel large deletions in the human alpha-globin gene cluster: Clarifying the HS-40 long-range regulatory role in the native chromosome environment. [J] . Coelho A, Picanco I, Seuanes F, Blood cells, molecules and diseases . 2010 ,第2期

机译：人类α-珠蛋白基因簇中的新型大缺失：阐明HS-40在天然染色体环境中的远程调节作用。
4. Method for Identifying HbCS Variant in Alpha Globin denes Causing AIpha-Thalassaemia Disease [C] . Ngoc Bao Tran, Hue Thi Nguyen International Conference on the Development of Biomedical Engineering in Vietnam . 2018

机译：鉴定α球蛋白的HBCS变体的方法，导致AIVHA-Thalassemia疾病
5. Hydrops fetalis caused by homozygous alpha thalassemia: A DNP case study project [D] . Redoblado, Erlinda B. 2015

机译：纯合α地中海贫血引起的胎儿水肿：DNP案例研究项目
6. Compensatory increase in alpha 1-globin gene expression in individuals heterozygous for the alpha-thalassemia-2 deletion. [O] . S A Liebhaber, F E Cash, D M Main 1985

机译：对于α-地中海贫血2缺失杂合的个体中α1-球蛋白基因表达的补偿性增加。
7. Alpha-thalassemia caused by a large (62 kb) deletion upstream of the human alpha globin gene cluster [O] . CS Hatton, AO Wilkie, HC Drysdale, 1990

机译：由人α球蛋白基因集群的上游缺失（62 kB）缺失引起的α-血症
8. Changes in Expression of Murine alpha- and beta-Globin Genes During Development [R] . Popp, R. A. , D'Surney, S. J. , Wawrzyniak, C. J. 1986

机译：小鼠α-和β-珠蛋白基因在发育过程中表达的变化

A novel deletion causing alpha thalassemia clarifies the importance of the major human alpha globin regulatory element.

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