Abstract
摘要
相似文献
1
The alpha thalassemia genes.α地中海贫血基因
J Med Assoc Thai. 1970 Oct;53(10):677-86.
2
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.
3
Various aspects of alpha-thalassemia.α地中海贫血的各个方面。
Ann N Y Acad Sci. 1974;232(0):152-8. doi: 10.1111/j.1749-6632.1974.tb20580.x.
4
Pathogenesis of the thalassemia syndromes.地中海贫血综合征的发病机制。
Pathobiol Annu. 1980;10:1-33.
5
Alpha-thalassemia in Northern Thailand.泰国北部的α地中海贫血
Am J Hum Genet. 1970 Nov;22(6):645-51.
6
Hemoglobin inclusions in heterozygous alpha-thalassemia according to their alpha-globin genotype.
Acta Haematol. 1984;72(1):34-6. doi: 10.1159/000206353.
7
[Ophthalmological manifestations of the hemoglobinopathies].[血红蛋白病的眼科表现]
Arch Ophtalmol Rev Gen Ophtalmol. 1974 Jan;34(1):5-30.
8
High prevalence of alpha-thalassemia in a black population of Brazil.巴西黑人人群中α地中海贫血的高患病率。
Hemoglobin. 1991;15(4):309-11. doi: 10.3109/03630269109027884.
9
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
Blut. 1974 May;28(5):326-36. doi: 10.1007/BF01631520.
10
Duplicated alpha-chain genes in Hopkins-2 haemoglobin of man and evidence for unequal crossing over between them.人类霍普金斯 - 2血红蛋白中的重复α - 珠蛋白基因及其之间不等交换的证据。
Nat New Biol. 1972 May 17;237(72):90-4. doi: 10.1038/newbio237090a0.
引用本文的文献
1
An unusual hemoglobin anomaly and its relation to alpha-thalassemia and hemoglobin-H disease.一种不寻常的血红蛋白异常及其与α地中海贫血和血红蛋白H病的关系。
J Clin Invest. 1971 Aug;50(8):1628-36. doi: 10.1172/JCI106651.
2
Haemoglobin synthesis in 28 obligatory cases for alpha-thalassemia traits.28例α地中海贫血特征的必需病例中的血红蛋白合成。
Humangenetik. 1975 Sep 10;29(2):121-6. doi: 10.1007/BF00430348.
Zotero 插件