Umbilical Cord Blood Screening for the Detection of Common Deletional Mutations of α-Thalassemia in Bangladesh-Reference-Cited by-同舟云学术

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Umbilical Cord Blood Screening for the Detection of Common Deletional Mutations of α-Thalassemia in Bangladesh

Published:2020-05-03 Issue:3 Volume:44 Page:201-210
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Anwar Saeed¹^ORCID,Taslem Mourosi Jarin¹^ORCID,Hasan Md. Kamrul²³^ORCID,Hosen Mohammad Jakir¹^ORCID,Miah Md. Faruque¹^ORCID

Affiliation:

1. Department of Genetic Engineering and Biotechnology, School of Life Sciences, Shahjalal University of Science and Technology, Sylhet, Bangladesh;

2. Department of Biochemistry and Molecular Biology, Tejgaon College, National University of Bangladesh, Gazipur, Bangladesh;

3. Department of Public Health, School of Health and Life Sciences, North South University, Dhaka, Bangladesh

Publisher

Informa UK Limited

Subject

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

Link

https://www.tandfonline.com/doi/pdf/10.1080/03630269.2020.1784755

Reference66 articles.

1. Thalassaemia

2. α-thalassaemia

3. Global epidemiology of haemoglobin disorders and derived service indicators

4. Clinical Manifestations of -Thalassemia

Cited by 5 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. β-Thalassemia in Bangladesh: Current Status and Future Perspectives;Thalassemia Reports;2024-07-08

2. Current Status of Newborn Bloodspot Screening Worldwide 2024: A Comprehensive Review of Recent Activities (2020–2023);International Journal of Neonatal Screening;2024-05-23

3. Thalassemia and hemoglobinopathy prevalence in a community-based sample in Sylhet, Bangladesh;Orphanet Journal of Rare Diseases;2023-07-19

4. α- and β-Globin Gene Mutations in Individuals with Hemoglobinopathies in the Chattogram and Sylhet Regions of Bangladesh;Hemoglobin;2023-01-02

5. Genetic counseling in the context of Bangladesh: current scenario, challenges, and a framework for genetic service implementation;Orphanet Journal of Rare Diseases;2021-04-09

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