Genetic variants of HBS1L-MYB with Hb subtypes level among Filipino β°-deletion carriers co-inherited with −α3.7 deletion thalassaemia-Reference-Cited by-同舟云学术

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Genetic variants of HBS1L-MYB with Hb subtypes level among Filipino β°-deletion carriers co-inherited with −α3.7 deletion thalassaemia

Published:2020-12 Issue: Volume:26 Page:100769
ISSN:2214-5400
Container-title:Meta Gene
language:en
Short-container-title:Meta Gene

Author:

Lim Lay Ngor,Teh Lai Kuan^ORCID,Yu Koh Sam,Chua Shi Min,George Elizabeth,Lai Mei I,Wong Lily

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference38 articles.

1. Genetic recombination as a major cause of mutagenesis in the human globin gene clusters;Borg;Clin. Biochem.,2009

2. Simplified multiplex-PCR diagnosis of common southeast Asian deletional determinants of α-thalassemia;Chong;Clin. Chem.,2000

3. Single-tube multiplex-PCR screen for common deletional determinants of α-thalassemia;Chong;Blood,2000

4. HPLC studies in hemoglobinopathies;Colah;Indian J. Pediatr.,2007

5. Genetic variation on chromosome 6 influences F cell levels in healthy individuals of African descent and HbF levels in sickle cell patients;Creary;PLoS One,2009

Cited by 1 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. Single Nucleotide Polymorphisms in XMN1-HBG2, HBS1L-MYB, and BCL11A and Their Relation to High Fetal Hemoglobin Levels That Alleviate Anemia;Diagnostics;2022-06-02

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