Molecular Characterization ofδ-Thalassemia in Iran-Reference-Cited by-同舟云学术

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Molecular Characterization ofδ-Thalassemia in Iran

Published:2016-01-02 Issue:1 Volume:40 Page:44-47
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Kordafshari Alireza,Amirian Azam,Zeinali Sirous,Valaei Atefeh,Maryami Fereshteh,Karimipoor Morteza

Publisher

Informa UK Limited

Subject

Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology

Link

http://www.tandfonline.com/doi/pdf/10.3109/03630269.2015.1092982

Reference21 articles.

1. The Thalassaemia Syndromes

2. Homozygous Delta-Thalassemia First Discovered in Japanese Family With Hereditary Persistence of Fetal Hemoglobin

3. Identification of four novel delta-globin gene mutations in Greek Cypriots using polymerase chain reaction and automated fluorescence- based DNA sequence analysis

Cited by 9 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. A New δ-Globin Gene Variant: Hb A2-Yulin [δ46(CD5)Gly→Arg, HBD : C.139G > A];Hemoglobin;2024-03-03

2. The blood count as a compass to navigate in the ever-changing landscape of the carrier state of hemoglobinopathies: a single-center Italian experience;Frontiers in Pediatrics;2023-10-06

3. Mutational spectrum of HBD gene in the Chinese population: Description of 36 mutations including 11 novel variants;International Journal of Laboratory Hematology;2023-08-22

4. Prospective screening for δ-hemoglobinopathies associated with decreased hemoglobin A2 levels or hemoglobin A2 variants: A single center experience;Clinica Chimica Acta;2023-07

5. A New Mutation, Hb A₂-Canakkale [δ10(A7)Ala→Val; HBD: c.32C>T], and Other Well-Known δ Variants Identified in a Selected Cohort with Low Hb A₂ Levels;Hemoglobin;2022-03-04

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