AnAluElement-Mediated 28.5 kb α-Thalassemia Deletion Found in a Chinese Family
Author:
Publisher
Informa UK Limited
Subject
Biochemistry, medical,Clinical Biochemistry,Genetics(clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.3109/03630269.2014.976793
Reference29 articles.
1. The Alpha Thalassaemias
2. Alpha thalassemia major—new mutations, intrauterine management, and outcomes
3. The involvement of Alu repeats in recombination events at the α-globin gene cluster: characterization of two α°-thalassaemia deletion breakpoints
4. Heterogeneity of the egammadeltabeta-thalassaemias: characterization of three novel English deletions
5. A review of the molecular genetics of the human alpha-globin gene cluster
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3. Characterization of two novel Alu element-mediated α-globin gene cluster deletions causing α0-thalassemia by targeted next-generation sequencing;Molecular Genetics and Genomics;2020-01-02
4. Mobile Elements in the Human Genome: Implications for Disease;eLS;2017-12-15
5. Characterization of a Large Novel α-Globin Gene Cluster Deletion Causing α0-Thalassemia in a Chinese Family;Hemoglobin;2017-11-02
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