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.1365-2141.1987.00369.x/fullpdf
Reference21 articles.
1. Structurally diverse molecular deletions in the β-globin gene cluster exhibit an identical phenotype on interaction with the βs-gene;Anagnou;Blood,1985
2. Differences between the levels of Gγ chain in the fetal hemoglobin of two types of HPFH are linked with a variation in DNA sequence;Bakioglu;Biochemical Genetics,1986
3. The GenBank genetic sequence databank;Bilofsky;Nucleic Acids Research,1986
4. The 18- to 23-kb deletion of the Macedonian δβ-thalassemia includes the entire δ and β globin genes;Efremov;Blood,1986
5. Lambda replacement vectors carrying polylinker sequences;Frischauf;Journal of Molecular Biology,1983
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