Sickle cell anemia as a syndrome: A review of diagnostic features-Reference-Cited by-同舟云学术

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Sickle cell anemia as a syndrome: A review of diagnostic features

Published:1979-04 Issue:2 Volume:6 Page:173-184
ISSN:0361-8609
Container-title:American Journal of Hematology
language:en
Short-container-title:Am. J. Hematol.

Author:

Huisman Titus H. J.

Publisher

Wiley

Subject

Hematology

Reference75 articles.

1. : “The Hemoglobinopathies, Techniques of Identification.” New York: Marcel Dekker, 1977.

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

3. Sickle cell anemia and trait in Southern India: Further studies

4. Abnormal human haemoglobins V. Chemical investigation of haemoglobins A, G, C, X from one individual

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2. Frequencies and phenotypic consequences of association of α- and β-thalassemia alleles with sickle-cell disease in Bahrain;International Journal of Laboratory Hematology;2016-12-16

3. Fetal haemoglobin in sickle-cell disease: from genetic epidemiology to new therapeutic strategies;The Lancet;2016-06

4. Erythroid differentiation ability of butyric acid analogues: Identification of basal chemical structures of new inducers of foetal haemoglobin;European Journal of Pharmacology;2015-04

5. Clinical, hematological and genetic features of sickle-cell anemia and sickle cell-β thalassemia in a Brazilian population;Clinical Genetics;2008-04-23

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