Is Hb A2Elevated in Adults with Sickle-A-Thalassemi (βS/βS; -α/-α)
Author:
Publisher
Informa UK Limited
Subject
Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.3109/03630269708993127
Reference42 articles.
1. A New Sickling Disorder Resulting from Interaction of the Genes for Haemoglobin S and α-Thalassaemia
2. Benign Obstetric History in Women with Sickle-cell Anaemia Associated with -Thalassaemia
3. Detection of sickle alpha- or beta0-thalassemia by studies of globin biosynthesis
4. Failure of the alpha-thalassemia gene to decrease the severity of sickle cell anemia
5. Sickle cell syndromes
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1. THE EFFECT OF ALPHA THALASSEMIA, HBF and HBC ON HAEMATOLOGICAL PARAMETERS OF SICKLE CELL DISEASE PATIENTS IN IBADAN, NIGERIA.;Mediterranean Journal of Hematology and Infectious Diseases;2022-01-01
2. Sickle cell haemoglobin and its interactions with other variant haemoglobins and with thalassaemias;Haemoglobinopathy Diagnosis;2020-02-28
3. Effect of Assorted Globin Haplotypes and α-Thalassemia on the Clinical Heterogeneity of Hb S-β-Thalassemia;Hemoglobin;2018-07-04
4. Sickle cell disease: Classification of clinical complications and approaches to preventive and therapeutic management;Clinical Hemorheology and Microcirculation;2018-03-28
5. 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
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