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Guidelines for investigation of the alpha and beta thalassaemia traits. The Thalassaemia Working Party of the BCSH General Haematology Task Force.

出版信息

J Clin Pathol. 1994 Apr;47(4):289-95. doi: 10.1136/jcp.47.4.289.

DOI:10.1136/jcp.47.4.289
PMID:7517954
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC501928/
Abstract
摘要

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本文引用的文献

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Estimation of small percentages of foetal haemoglobin.微量胎儿血红蛋白的测定。
Nature. 1959 Dec 12;184(Suppl 24):1877-8. doi: 10.1038/1841877a0.
2
Determination of low percentages of fetal hemoglobin in blood of normal children.正常儿童血液中低百分比胎儿血红蛋白的测定。
AMA J Dis Child. 1956 Dec;92(6):588-91. doi: 10.1001/archpedi.1956.02060030582007.
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The effect of iron deficiency on the levels of hemoglobins A2 and E.缺铁对血红蛋白A2和E水平的影响。
J Lab Clin Med. 1968 Jan;71(1):85-91.
4
Reliable routine estimation of small amounts of foetal haemoglobin by alkali denaturation.通过碱变性对少量胎儿血红蛋白进行可靠的常规估算。
J Clin Pathol. 1972 Aug;25(8):738-40. doi: 10.1136/jcp.25.8.738.
5
Serum iron and unsaturated iron-binding capacity in the -thalassaemia trait: their relation to the levels of haemoglobins A, A 2 , and F.β地中海贫血特征患者的血清铁与不饱和铁结合能力：它们与血红蛋白A、A2和F水平的关系。
J Med Genet. 1972 Jun;9(2):154-9. doi: 10.1136/jmg.9.2.154.
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A review of the molecular genetics of the human alpha-globin gene cluster.人类α-珠蛋白基因簇的分子遗传学综述。
Blood. 1989 Apr;73(5):1081-104.
7
Discriminant functions.判别函数。
Blood Cells. 1989;15(3):463-71; discussion 472-3.
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Automated measurement of red blood cell microcytosis and hypochromia in iron deficiency and beta-thalassemia trait.缺铁性贫血和β地中海贫血特征中红细胞小红细胞症和低色素症的自动测量
Arch Pathol Lab Med. 1992 Jan;116(1):84-9.
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A PCR-based strategy to detect the common severe determinants of alpha thalassaemia.一种基于聚合酶链反应的策略，用于检测α地中海贫血的常见严重决定因素。
Br J Haematol. 1992 May;81(1):104-8. doi: 10.1111/j.1365-2141.1992.tb08180.x.
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Hemoglobin A2 levels in health and various hematologic disorders.
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