Iranian patients with hemoglobin H disease: genotype–phenotype correlation
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics,Molecular Biology,General Medicine
Link
http://link.springer.com/content/pdf/10.1007/s11033-019-04955-9.pdf
Reference26 articles.
1. Alkindi SS et al (2013) A stepwise α-thalassemia screening strategy in high-prevalence areas. Eur J Haematol 91(2):164–169
2. Karamzade A et al (2014) α-Globin gene mutations in Isfahan province. Iran Hemoglobin 38(3):161–164
3. Vichinsky EP (2009) Alpha thalassemia major—new mutations, intrauterine management, and outcomes. ASH Educ Program Book 2009(1):35–41
4. Chen FE et al (2000) Genetic and clinical features of hemoglobin H disease in Chinese patients. N Engl J Med 343(8):544–550
5. Waye JS et al (2001) Hemoglobin H (Hb H) disease in Canada: molecular diagnosis and review of 116 cases. Am J Hematol 68(1):11–15
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2. Evaluation of Clinical, Laboratory Characteristics of Hemoglobin H Disease Patients from 2002 to 2022 Referred to Thalassemia Center, Bu-Ali Sina Hospital in Sari North of Iran;2024-02-28
3. First report of a rare complex rearrangement in the α-globin gene cluster causing a novel 16.8Kb deletion;2023-12-19
4. Genotype–phenotype correlation in patients with deletional and nondeletional mutations of Hb H disease in Southwest of Iran;Scientific Reports;2022-03-22
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