Quantities of αQ chain variants in heterozygotes with and without a concomitant β-thalassemia trait-Reference-Cited by-同舟云学术

Quantities of αQ chain variants in heterozygotes with and without a concomitant β-thalassemia trait

Published:1994-01 Issue:1 Volume:45 Page:91-93
ISSN:0361-8609
Container-title:American Journal of Hematology
language:en
Short-container-title:Am. J. Hematol.

Author:

Qin W.-B.,Baysal E.,Wong K. F.,Molchanova T. P.,Pobedimskaya D. D.,Sharma S.,Wilson J. B.,Huisman T. H. J.

Publisher

Wiley

Subject

Hematology

Reference9 articles.

1. : “The Thalassaemia Syndromes”. 3rd ed. Oxford: Blackwell Scientific Publications, 1981.

2. , , : Conventional isoelectric focusing and immobilized pH gradients for hemoglobin separation and identification. In (ed): “The Hemoglobinopathies.” Edinburgh: Churchill Livingstone, 1986, p 47.

3. High-performance liquid chromatographic separation of human haemoglobins

4. Separation of tryptic peptides of normal and abnormal a, β, γ, and δ hemoglobin chains by high-performance liquid chromatography

5. Hb H disease in a Turkish family resulting from the interaction of a deletional α-thalassaemia-1 and a newly discovered poly A mutation

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