地中海贫血：基因型与表型 - Suppr

Thalassemia: genotypes and phenotypes.

作者信息

Loukopoulos D

机构信息

First Department of Medicine, University of Athens, Laikon Hospital, Greece.

出版信息

Ann Hematol. 1991 May;62(5):145-50. doi: 10.1007/BF01703138.

DOI:10.1007/BF01703138

PMID:2049458

Abstract

摘要

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本文引用的文献

Heterozygous Beta thalassemia: balanced globin synthesis in bone marrow cells.

Science. 1970 Mar 13;167(3924):1513-4. doi: 10.1126/science.167.3924.1513.

Inclusions of hemoglobin erythroblasts and erythrocytes of thalassemia.

Blood. 1963 Jan;21:21-32.

Globin chain synthesis analysis in obligate beta 0-thalassemia heterozygotes with isolated increase of hemoglobin A2 levels.

Nouv Rev Fr Hematol (1978). 1981;23(4):193-5.

Globin structural mutant alpha 125Leu leads to Pro is a novel cause of alpha-thalassaemia.

Nature. 1982 Apr 29;296(5860):864-5. doi: 10.1038/296864a0.

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Alpha-thalassaemia caused by a polyadenylation signal mutation.

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The interaction of alpha thalassaemia with heterozygous beta thalassaemia.

Br J Haematol. 1982 Nov;52(3):465-73. doi: 10.1111/j.1365-2141.1982.tb03916.x.

Linkage of beta-thalassaemia mutations and beta-globin gene polymorphisms with DNA polymorphisms in human beta-globin gene cluster.

Nature. 1982 Apr 15;296(5858):627-31. doi: 10.1038/296627a0.

Base substitution in an intervening sequence of a beta+-thalassemic human globin gene.

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Thalassemia: genotypes and phenotypes.

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Thalassemia: genotypes and phenotypes.

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