Molecular characterisation of beta thalassaemia heterozygotes in Brazil.
作者信息
Martins C S, Ramalho A S, Sonati M F, Gonçalves M S, Costa F F
出版信息
J Med Genet. 1993 Sep;30(9):797-8. doi: 10.1136/jmg.30.9.797-b.
Abstract
摘要
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本文引用的文献
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Hereditary haemoglobin disorders in Brazil.
Trans R Soc Trop Med Hyg. 1985;79(3):385-8. doi: 10.1016/0035-9203(85)90389-x.
2
3
The thalassemia syndromes: molecular basis and prenatal diagnosis in 1990.地中海贫血综合征：1990年的分子基础与产前诊断
Semin Hematol. 1990 Jul;27(3):209-28.
4
Beta-thalassemia intermedia and IVS-1 NT6 homozygosis in Brazil.巴西的中间型β地中海贫血与IVS-1 NT6纯合子状态
Braz J Med Biol Res. 1991;24(2):157-61.
5
Bone marrow transplantation using voluntary donors. Role of European Secretariat.使用自愿捐献者的骨髓移植。欧洲秘书处的作用。
Nouv Rev Fr Hematol (1978). 1991;33(6):441-3.
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A novel beta zero-thalassaemia mutation (codon 15, TGG----TGA) is prevalent in a population of central Portugal.一种新的β0地中海贫血突变（密码子15，TGG----TGA）在葡萄牙中部人群中很常见。
Br J Haematol. 1992 Apr;80(4):567-8. doi: 10.1111/j.1365-2141.1992.tb04581.x.
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