Genetic counseling and prenatal decision for hemoglobin H disease caused by the rare α2 codon 30 (-GAG) (HBA2: c.91_93delGAG) mutation and the SEA deletion: Case series study
Author:
Publisher
Elsevier BV
Subject
Obstetrics and Gynecology
Reference14 articles.
1. Thalassaemia;Taher;Lancet,2018
2. Molecular characterization of Hb H disease in southern Thailand;Nittayaboon;Int J Hematol,2018
3. Phenotype and genotype in a cohort of 312 adult patients with nontransfusion-dependent thalassemia in Northeast Thailand;Prayalaw;Acta Haematol,2016
4. Two alpha1-globin gene point mutations causing severe Hb H disease;Jiang;Hemoglobin,2017
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1. Molecular analysis and clinical significance of hemoglobin Quong Sze in Huizhou city, Southern China;Taiwanese Journal of Obstetrics and Gynecology;2023-09
2. A Case of Misdiagnosis Caused by the Coinheritance of Hb G-Siriraj [β7(A4)Glu→Lys; HBB: c.22G>A] and Hb H Disease;Hemoglobin;2022-11-02
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