The 12.6 kilobase DNA deletion in Dutch β°-thalassaemia
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.1987.tb02360.x/fullpdf
Reference21 articles.
1. Structurally diverse molecular deletions in the beta-globin gene cluster exhibit an identical phenotype on interaction with the beta S- gene
2. Differences between the levels of G? chain in the fetal hemoglobin in two types of hereditary persistence of fetal hemoglobin are linked with a variation in the DNA sequence
3. The GenBank genetic sequence databank
4. The 18- to 23-kb deletion of the Macedonian delta beta-thalassemia includes the entire delta and beta globin genes
5. Lambda replacement vectors carrying polylinker sequences
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2. Whole genome sequence-based haplotypes reveal a single origin of the 1393 bp HBB deletion;Journal of Medical Genetics;2020-01-30
3. Molecular basis of β thalassemia and potential therapeutic targets;Blood Cells, Molecules, and Diseases;2018-05
4. Characterization of Two Novel Deletions Involving the 5′ Region of the β-Globin Gene;Hemoglobin;2017-11-02
5. Genetic Basis and Genetic Modifiers of β-Thalassemia and Sickle Cell Disease;Advances in Experimental Medicine and Biology;2017
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