Characterizing a Cohort of α-Thalassemia Couples Collected During Screening for Hemoglobinopathies: 14 Years of an Iranian Experience-Reference-Cited by-同舟云学术

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Characterizing a Cohort of α-Thalassemia Couples Collected During Screening for Hemoglobinopathies: 14 Years of an Iranian Experience

Published:2014-05-14 Issue:3 Volume:38 Page:153-157
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Hafezi-Nejad Nima,Khosravi Mohsen,Bayat Nooshin,Kariminejad Ariana,Hadavi Valeh,Oberkanins Christian,Azarkeivan Azita,Najmabadi Hossein

Publisher

Informa UK Limited

Subject

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

Link

http://www.tandfonline.com/doi/pdf/10.3109/03630269.2014.909365

Reference33 articles.

1. Elucidating the spectrum of -thalassemia mutations in Iran

2. Molecular Analyses of β-Thalassa in Iran

3. MOLECULAR SPECTRUM OF β-THALASSEMIA IN THE IRANIAN PROVINCE OF HORMOZGAN

4. THE β-THALASSEMIA MUTATION SPECTRUM IN THE IRANIAN POPULATION

Cited by 7 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. Problem of borderline hemoglobin A2 levels in an Iranian population with a high prevalence of α- and β-thalassemia carriers;Egyptian Journal of Medical Human Genetics;2022-03-11

2. Quality of Life and Related Paraclinical Factors in Iranian Patients with Transfusion-Dependent Thalassemia;Journal of Environmental and Public Health;2021-08-18

3. Heterozygosity for the Novel HBA2: c.*91_*92delTA Polyadenylation Site Variant on the α2-Globin Gene Expanding the Genetic Spectrum of α-Thalassemia in Iran;Hemoglobin;2020-10-14

4. α-Globin Genotypes Associated with Hb H Disease: A Report from Oman and a Review of the Literature from the Eastern Mediterranean Region;Hemoglobin;2020-01-02

5. Iranian patients with hemoglobin H disease: genotype–phenotype correlation;Molecular Biology Reports;2019-07-04

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