Various aspects of alpha-thalassemia.
作者信息
Lehmann H, Lang A
出版信息
Ann N Y Acad Sci. 1974;232(0):152-8. doi: 10.1111/j.1749-6632.1974.tb20580.x.
Abstract
摘要
相似文献
1
Various aspects of alpha-thalassemia.α地中海贫血的各个方面。
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A new form of beta-thalassemia trait.一种新型的β地中海贫血特征。
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Is haemoglobin G Philadelphia linked to -thalassaemia?血红蛋白G费城型与β地中海贫血有关联吗？
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Absence of haemoglobin A in an individual simultaneously heterozygous in the genes for hereditary persistence of foetal haemoglobin and beta-thalassemia.个体同时在胎儿血红蛋白遗传性持续和β地中海贫血基因上呈杂合状态时血红蛋白A缺失。
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The interaction of alpha-thalassemia and homozygous sickle-cell disease.α地中海贫血与纯合子镰状细胞病的相互作用。
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The silent carrier of beta thalassemia.β地中海贫血的沉默携带者
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引用本文的文献
1
Diagnosis of alpha-thalassemia trait from Coulter Counter 'S' indices.通过库尔特计数器“S”指数诊断α地中海贫血特征。
J Clin Pathol. 1977 Sep;30(9):884-9. doi: 10.1136/jcp.30.9.884.
2
Postsynthetic deamidation of hemoglobin Providence (beta 82 Lys replaced by Asn, Asp) and its effect on oxygen transport.血红蛋白普罗维登斯的合成后脱酰胺作用（β82位赖氨酸被天冬酰胺、天冬氨酸取代）及其对氧运输的影响。
J Clin Invest. 1977 Apr;59(4):652-8. doi: 10.1172/JCI108683.
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