Analysis of Mrna from Red Cells of Patients with Thalassemia and Hemoglobin Variants
Author:
Publisher
Informa UK Limited
Subject
Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.3109/03630269708993129
Reference39 articles.
1. Human α‐Thalassemia syndromes: Detection of molecular defects
2. Advances in the Prenatal and Molecular Diagnosis of the Hemoglobinopathies and Thalassemias
3. The -158 (C-->T) promoter mutation is responsible for the increased transcription of the 3' gamma gene in the Atlanta type of hereditary persistence of fetal hemoglobin
4. γ-mRNA and Hb F levels in β-thalassaemia
5. The differences in quantities of α2-and α1-globin gene variants in heterozygotes
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