Alpha thalassaemia due to non-deletional mutations on the -3.7 alpha globin fusion gene: laboratory diagnosis and clinical importance
Author:
Publisher
Elsevier BV
Subject
Pathology and Forensic Medicine
Reference10 articles.
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3. Hb Bleuland [alpha108(G15)Thr->Asn, ACC->AAC (alpha2)]: a new abnormal hemoglobin associated with a mild alphathalassemia phenotype;Harteveld;Hemoglobin,2006
4. Locus assignment of human alpha globin mutations by selective amplification and direct sequencing;Dode;Br J Haematol,1990
5. A rapid and reliable 7-deletion multiplex polymerase chain reaction assay for alpha-thalassemia;Tan;Blood,2001
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1. Molecular and Haematological Characteristics of alpha-Thalassemia Deletions in Yogyakarta Special Region, Indonesia;Reports of Biochemistry and Molecular Biology;2021-11-01
2. Loss of alpha‐globin genes in human subjects is associated with improved nitric oxide‐mediated vascular perfusion;American Journal of Hematology;2020-12-12
3. Co-inheritance of alpha globin gene deletion lowering serum iron level in female beta thalassemia patients;Molecular Biology Reports;2019-11-08
4. C>A substitution in NT 46 of the 3’ UTR region (the α complex protected region) of the alpha-1 globin gene: a non-deletional mutation or polymorphism?;Journal of Clinical Pathology;2019-08-21
5. The ‑α3.7 deletion in α‑globin genes increases the concentration of fetal hemoglobin and hemoglobin A2 in a Saudi Arabian population;Molecular Medicine Reports;2017-11-13
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