The association of sickle cell anemia with heterozygous and homozygous α-thalassemia-2: In vitro HB chain synthesis-Reference-Cited by-同舟云学术

The association of sickle cell anemia with heterozygous and homozygous α-thalassemia-2: In vitro HB chain synthesis

Published:1979-04 Issue:2 Volume:6 Page:91-106
ISSN:0361-8609
Container-title:American Journal of Hematology
language:en
Short-container-title:Am. J. Hematol.

Author:

Felice A. E.,Webber B.,Miller A.,Mayson S. M.,Harris H. F.,Henson J. B.,Gravely M. E.,Huisman T. H. J.

Publisher

Wiley

Subject

Hematology

Reference30 articles.

1. Hemoglobin α Chain Deficiency in Black Children with Variable Quantities of Hemoglobin Bart's at Birth

2. Studies on the Proportion and Synthesis of Haemoglobin G Philadelphia in Red Cells of Heterozygotes, a Homozygote, and a Heterozygote for both Haemoglobin G and α Thalassaemia

3. Alpha-thalassemia

4. Trimodality in the proportion of hemoglobin G Philadelphia in heterozygotes: evidence for heterogeneity in the number of human alpha chain loci.

5. , , , , : Post-translational control of human hemoglobin synthesis. The number of α chain genes and the synthesis of Hb S. In (ed): “The Red Cell.” New York: Alan R. Liss, 1978, p 131.

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