Novel 31.2 kbα0Deletion in a Palestinian Family withα-Thalassemia-Reference-Cited by-同舟云学术

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Novel 31.2 kbα0Deletion in a Palestinian Family withα-Thalassemia

Published:2015-06-26 Issue:5 Volume:39 Page:346-349
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Brieghel Christian,Birgens Henrik,Frederiksen Henrik,Hertz Jens M.,Steenhof Maria,Petersen Jesper

Publisher

Informa UK Limited

Subject

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

Link

http://www.tandfonline.com/doi/pdf/10.3109/03630269.2015.1054512

Reference15 articles.

1. α-thalassaemia

2. The α-Thalassemias

3. Epidemiological profile of common haemoglobinopathies in Arab countries

4. The Molecular Basis of -Thalassemia

5. Rapid detection of α-thalassaemia deletions and α-globin gene triplication by multiplex polymerase chain reactions

Cited by 4 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. Alpha-Thalassemia in Southern Italy: Characterization of Five New Deletions Removing the Alpha-Globin Gene Cluster;International Journal of Molecular Sciences;2023-01-30

2. Detection of hemoglobin H disease by long molecule sequencing;Journal of Clinical Laboratory Analysis;2022-09-04

3. Characterization of a Large Novel α-Globin Gene Cluster Deletion Causing α0-Thalassemia in a Chinese Family;Hemoglobin;2017-11-02

4. Rare α0-thalassemia deletions detected by MLPA in five unrelated Brazilian patients;Genetics and Molecular Biology;2017-10-02

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