A large cohort of β+-thalassemia in Thailand: Molecular, hematological and diagnostic considerations-Reference-Cited by-同舟云学术

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A large cohort of β+-thalassemia in Thailand: Molecular, hematological and diagnostic considerations

Published:2015-02 Issue:2 Volume:54 Page:164-169
ISSN:1079-9796
Container-title:Blood Cells, Molecules, and Diseases
language:en
Short-container-title:Blood Cells, Molecules, and Diseases

Author:

Yamsri Supawadee,Singha Kritsada,Prajantasen Thanet,Taweenan Wachiraporn,Fucharoen Goonnapa,Sanchaisuriya Kanokwan,Fucharoen Supan

Funder

National Research University

Office of the Higher Education Commission, Ministry of Education, Thailand

Thailand Research Fund

Publisher

Elsevier BV

Subject

Cell Biology,Hematology,Molecular Biology,Molecular Medicine

Reference32 articles.

1. The Thalassemia Syndromes;Weatherall,2001

2. Hemoglobinopathies in Southeast Asia;Fucharoen;Hemoglobin,1987

3. Micromapping of thalassemia and hemoglobinopathies in different regions of northeast Thailand and Vientaine, Laos People's Democratic Republic;Tritipsombat;Hemoglobin,2012

4. DNA polymorphisms at the BCL11A, HBS1L-MYB, and beta-globin loci associate with fetal hemoglobin levels and pain crises in sickle cell disease;Lettre;Proc. Natl. Acad. Sci. U. S. A.,2008

5. BCL11A is a major HbF quantitative trait locus in three different populations with beta-hemoglobinopathies;Sedgewick;Blood Cells Mol. Dis.,2008

Cited by 31 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. Clinical characteristics, laboratory features and genetic profile of hemoglobin E (HBB:c.79 G > A)/β (nucleotide -28 A > G) (HBB:c.-78 A > G) -thalassemia subjects identified from community- and hospital-recruited cohorts;Blood Cells, Molecules, and Diseases;2024-11

2. The Importance of Molecular Biological Analysis for the Laboratory Diagnostic of Homozygous Haemoglobin Malay;Balkan Journal of Medical Genetics;2024-06-01

3. Interaction of Thalassemia and Hb Variants in Southeast Asia: Genotype-Phenotype Relationship;Thalassemia Syndromes - New Insights and Transfusion Modalities;2023-11-22

4. Molecular understanding of unusual HbE-β ⁺ -thalassemia with Hb phenotype similar to HbE heterozygote: simple and rapid differentiation using HbE levels;Annals of Medicine;2023-10-10

5. Seroprevalence of toxoplasmosis related with uric acid in B-thalassemia major patients;Sumer 1;2023-08-15

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