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A silent composite hemoglobinopathy characterized by gene sequencing.

A. Zorai** 1 I. Moumni** 2 I. Benmansour 2 D. Chaouachi 2 A. Ghanem 3 S. Abbes 2, 3, * 
Abstract : We report the case of a 35-year-old Tunisian women with a chronic anemia non investigated for a long time. Laboratory analysis using advanced technology of DNA sequencing revealed a compound heterozygote for Hb O Arab and cd 39 beta degrees-thalassemia. It's the first time that such a genotype has been characterized by gene sequencing.
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Submitted on : Saturday, May 11, 2013 - 9:20:17 PM
Last modification on : Wednesday, October 28, 2020 - 9:52:03 AM
Long-term archiving on: : Monday, August 12, 2013 - 5:20:07 AM


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  • HAL Id : pasteur-00821691, version 1
  • PUBMED : 23461145



A. Zorai**, I. Moumni**, I. Benmansour, D. Chaouachi, A. Ghanem, et al.. A silent composite hemoglobinopathy characterized by gene sequencing.. Archives de l'Institut Pasteur de Tunis, 2011, 88 (1-4), pp.67-70. ⟨pasteur-00821691⟩



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