Thalassaemia intermedia: a genetic study in 11 patients.
作者信息
Aksoy M
出版信息
J Med Genet. 1970 Mar;7(1):47-51. doi: 10.1136/jmg.7.1.47.
Abstract
摘要
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Delta beta-thalassaemia in two Turkish families.
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A METHOD FOR THE QUANTITATIVE DETERMINATION OF HGB A2.
Ann N Y Acad Sci. 1964 Oct 7;119:557-60. doi: 10.1111/j.1749-6632.1965.tb54056.x.
3
THE THALASSEMIA SYNDROMES. BIOCHEMICAL, GENETIC AND CLINICAL CONSIDERATIONS.地中海贫血综合征：生化、遗传及临床方面的考量
Am J Med. 1964 Jun;36:919-35.
4
[A simple staining test for the determination of glucose-6-phosphate dehydrogenase in human erythrocytes. (Modification of the "Motulsky test")].[一种用于测定人红细胞中葡萄糖-6-磷酸脱氢酶的简单染色试验。（“莫图尔斯基试验”的改良）]
Klin Wochenschr. 1962 Jun 15;40:649-53. doi: 10.1007/BF01479072.
5
Absence of haemoglobin A2 in an adult.成人血红蛋白A2缺失。
Nature. 1962 Sep 22;195:1215-6. doi: 10.1038/1951215a0.
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Thalassaemia minor with large amount of fetal haemoglobin: report of four cases.
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Qunatitative determination of the minor hemoglobin component Hb-A2 by DEAE-cellulose chromatography.
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The thalassaemia syndromes. II. Intermediate type of Cooley's anaemia. Study of a family.
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Zone electrophoresis in starch gels: group variations in the serum proteins of normal human adults.淀粉凝胶区带电泳：正常成年人血清蛋白的群体差异
Biochem J. 1955 Dec;61(4):629-41. doi: 10.1042/bj0610629.
10
New hemoglobin in normal adult blood.正常成人血液中的新型血红蛋白。
Science. 1955 Aug 12;122(3163):288. doi: 10.1126/science.122.3163.288.
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