A Number of Cases in Iran Presenting with Coinheritance of Hemoglobin-H Disease and Beta-Thalassemia Minor
Author:
Affiliation:
1. Hematology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran;
2. Hematology Research Center, Dastgheib Hospital, Shiraz University of Medical Sciences, Shiraz, Iran
Publisher
Informa UK Limited
Subject
Biochemistry, medical,Clinical Biochemistry,Genetics(clinical),Hematology
Link
https://www.tandfonline.com/doi/pdf/10.1080/03630269.2016.1220953
Reference11 articles.
1. Laboratory diagnosis of thalassemia
2. Thalassaemia
3. Beta-thalassemia
4. The α-Thalassemias
5. Hb H disease: clinical course and disease modifiers
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Prenatal diagnosis of a rare β ‐thalassemia gene -90 (C>T) ( HBB : c.‐140 C>T) mutation associated with deletional Hb H disease (‐‐ SEA /‐ α 4.2 );Molecular Genetics & Genomic Medicine;2020-09-03
2. Beta-Talasemia: Un mundo de complicaciones con nuevas alternativas de tratamiento.;Archivos de Medicina (Manizales);2019-03-10
3. Results of Coexistence of β-Thalassemia Minor in Hb H Disease Patients;Hemoglobin;2018-11-02
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