A novel deletion causing (εγδβ)° thalassaemia in a Chilean family
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2141.2003.04564.x/fullpdf
Reference23 articles.
1. A de novo deletion causing εγδβ-thalassemia in a Dutch patient;Abels;Acta Haematologica,1996
2. Molecular characterisation of a novel form of (Aγδβ)° thalassemia deletion with a 3′ breakpoint close to those of HPFH-3 and HPFH-4: insights into a common regulatory mechanism;Anagnou;Nucleic Acids Research,1988
3. Non-random association of polymorphic restriction sites in the β-globin gene cluster;Antonarakis;Proceedings of the National Academy of Sciences of the USA,1982
4. A distant gene deletion affects β-globin gene function in an atypical γδβ-thalassemia;Curtin;Journal of Clinical Investigation,1985
5. Two new large deletions resulting in εγδβ-thalassemia;Diaz-Chico;Acta Haematologica,1988
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