Rapid molecular identification of a rare β-globin gene deletion & its clinical implication
Author:
Publisher
Medknow
Subject
General Biochemistry, Genetics and Molecular Biology,General Medicine
Reference14 articles.
1. Burden of thalassemia in India: The road map for control;Colah;Pediatr Hematol Oncol,2017
2. Hemoglobin A2 (HbA2) has a measure of unreliability in diagnosing β-thalassemia trait (β-TT);Al-Amodi;Curr Med Res Opin,2018
3. The changing trends in prenatal diagnosis of hemoglobinopathies in India: The quest of a single center to reduce the burden of disease over three decades;Colah;Hemoglobin,2021
4. Multiplex ligation-dependent probe amplification screening of isolated increased HbF levels revealed three cases of novel rearrangements/deletions in the beta-globin gene cluster;Lee;Br J Haematol,2010
5. Harteveld CL, Voskamp A, Phylipsen M, Akkermans N, den Dunnen JT, White SJ, et al. Nine unknown rearrangements in 16p13.3 and 11p15.4 causing alpha- and beta-thalassaemia characterised by high resolution multiplex ligation-dependent probe amplification. J Med Genet 2005; 42 : 922-31.
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