Pathogenesis of the thalassemia syndromes.
作者信息
Benz E J, Forget B G
出版信息
Pathobiol Annu. 1980;10:1-33.
PMID:6160450
Abstract
摘要
相似文献
1
Pathogenesis of the thalassemia syndromes.地中海贫血综合征的发病机制。
Pathobiol Annu. 1980;10:1-33.
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Various aspects of alpha-thalassemia.α地中海贫血的各个方面。
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3
[Double heterozygous Hb O Arab/beta-thalassemia in a Tunisian child].[一名突尼斯儿童的双重杂合子 Hb O Arab/β地中海贫血]
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[Genetic study of thalassemia].[地中海贫血的基因研究]
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The present status of the heterogeneity of fetal hemoglobin in beta-thalassemia: an attempt to unify some observations in thalassemia and related conditions.β地中海贫血中胎儿血红蛋白异质性的现状：统一地中海贫血及相关病症中一些观察结果的尝试。
Ann N Y Acad Sci. 1974;232(0):107-24. doi: 10.1111/j.1749-6632.1974.tb20576.x.
6
Hemoglobin Lepore: its significance for thalassemia and clinical manifestations.血红蛋白Lepore：其对地中海贫血的意义及临床表现
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7
Thalassemia in Thailand.泰国的地中海贫血。
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Homozygous beta thalassemia in American Blacks: the problem of mild thalassemia.美国黑人中的纯合子β地中海贫血：轻度地中海贫血问题
J Lab Clin Med. 1973 Jun;81(6):857-66.
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[Double heterozygosity of Hb O ARAB/beta + thalassemia in an Algerian family].[一个阿尔及利亚家庭中Hb O ARAB/β+地中海贫血的双重杂合性]
Nouv Rev Fr Hematol (1978). 1982;24(5):289-94.
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[Heterozygous beta-thalassemia without icrease of hemoglobin A2].[血红蛋白A2无升高的杂合子β地中海贫血]
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引用本文的文献
1
Posttranscriptional defects in beta-globin messenger RNA metabolism in beta-thalassemia: abnormal accumulation of beta-messenger RNA precursor sequences.β地中海贫血中β-珠蛋白信使核糖核酸代谢的转录后缺陷：β-信使核糖核酸前体序列的异常积累
J Clin Invest. 1981 Dec;68(6):1529-38. doi: 10.1172/jci110407.
2
Molecular analysis of the beta-thalassemia phenotype associated with inheritance of hemoglobin E (alpha 2 beta2(26)Glu leads to Lys).与血红蛋白E（α2β2(26)谷氨酸突变为赖氨酸）遗传相关的β地中海贫血表型的分子分析
J Clin Invest. 1981 Jul;68(1):118-26. doi: 10.1172/jci110226.
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