Hemoglobinopathies and thalassemias. Abnormalities of hemoglobin structure, function, and synthesis.
作者信息
Honig G R
出版信息
Postgrad Med. 1974 May;55(5):77-83. doi: 10.1080/00325481.1974.11713755.
Abstract
摘要
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1
Hemoglobinopathies and thalassemias. Abnormalities of hemoglobin structure, function, and synthesis.血红蛋白病和地中海贫血。血红蛋白结构、功能及合成异常。
Postgrad Med. 1974 May;55(5):77-83. doi: 10.1080/00325481.1974.11713755.
2
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Chemical heterogeneity of fetal hemoglobin in subjects with sickle cell anemia, homozygous Hb-C disease, SC disease, and various combinations of hemoglobin variants.镰状细胞贫血、纯合子血红蛋白C病、血红蛋白SC病以及各种血红蛋白变异体组合的患者中胎儿血红蛋白的化学异质性。
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6
The molecular basis of hemoglobin disease.血红蛋白疾病的分子基础。
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7
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8
Laboratory diagnosis of hemoglobinopathies.血红蛋白病的实验室诊断
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The ratio of G gamma and A gamma chains of the hemoglobin F synthesized by BFU-E-derived colonies from blood of subjects with beta+ thalassemia and related hemoglobinopathies.来自β+地中海贫血及相关血红蛋白病患者血液中BFU-E衍生集落合成的血红蛋白F的Gγ链与Aγ链的比例。
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