Characterization of a Novel Deletion Causing β-Thalassemia Major in an Afghan Family-Reference-Cited by-同舟云学术

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Characterization of a Novel Deletion Causing β-Thalassemia Major in an Afghan Family

Published:2010-01 Issue:1 Volume:34 Page:110-114
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Gallienne Alice E.,Iberson Nicola M.,Dréau Hélène M.,Jackson Helen,Bignell Patricia A.,Old John M.,Schuh Anna,Henderson Shirley J.

Publisher

Informa UK Limited

Subject

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

Link

http://www.tandfonline.com/doi/pdf/10.3109/03630260903554803

Reference11 articles.

1. 3 β-Thalassaemia

2. The Thalassaemia Syndromes

3. Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification

4. Nine unknown rearrangements in 16p13.3 and 11p15.4 causing - and -thalassaemia characterised by high resolution multiplex ligation-dependent probe amplification

5. Molecular characterization of a high A2 beta thalassemia by direct sequencing of single strand enriched amplified genomic DNA

Cited by 6 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. Rapid molecular identification of a rare β-globin gene deletion & its clinical implication;Indian Journal of Medical Research;2022

2. Characterization and identification of Prachinburi β 0 ‐thalassemia: A novel‐60 kb deletion in beta globin gene related to high levels of Hb F in heterozygous state;International Journal of Laboratory Hematology;2021-03-18

3. Characterization of Two Novel Deletions Involving the 5′ Region of the β-Globin Gene;Hemoglobin;2017-11-02

4. Advances in detection of hemoglobinopathies;Clinica Chimica Acta;2015-01

5. Detection of Anti-Lepore Hb P-Nilotic by Multiplex Ligation-Dependent Probe Amplification;Hemoglobin;2012-03-02

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