Sickle Cell-Hemoglobin D Iran: A Benign Sickle Cell Syndrome
Author:
Publisher
Informa UK Limited
Subject
Biochemistry, medical,Clinical Biochemistry,Genetics(clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.3109/03630268208996934
Reference7 articles.
1. Screening Cord Bloods for Detection of Sickle Cell Disease in Jamaica
2. Haemoglobin D Iran: β222 Glutamic Acid→Glutamine (B4)
3. Comparison of Haematological Features of the β0and β+Thalassaemia Traits in Jamaican Negroes
4. The Ferrohemoglobin Solubility Test
5. Estimation of Small Percentages of Fœtal Hæmoglobin
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1. Hb D-Iran interference on HbA1c measurement;Clinical Chemistry and Laboratory Medicine (CCLM);2024-08-06
2. Non-Sickle Cell Structural Hemoglobinopathies;Decision Making Through Problem Based Learning in Hematology;2024
3. Compound heterozygote of Hb DIran [HBB: c.67G>C, β 22(B4) Glu>Gln] with β0-thalassemia [cds 41/42 (-CTTT)] from Eastern India;Hematology, Transfusion and Cell Therapy;2018-01
4. Comparison of the characteristics of two hemoglobin variants, Hb D-Iran and Hb E, eluting in the Hb A2 window;Blood Research;2017
5. Comments on: “Clinical, hematological and genetic data of a cohort of children with hemoglobin SD”;Revista Brasileira de Hematologia e Hemoterapia;2016-07
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