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Original article
Phenotypic evaluations of HBB:c.93-23T>C, a nucleotide substitution in the IVS I nt 108 of β-globin gene

Authors

  • Margherita Vinciguerra Department of Hematology for Rare Diseases of Blood and Blood-forming Organs, Laboratory for Molecular Diagnosis of Rare Diseases, Villa Sofia-Cervello Hospital, Palermo, Italy PubMed articlesGoogle scholar articles
  • Filippo Cassarà Department of Hematology for Rare Diseases of Blood and Blood-forming Organs, Laboratory for Molecular Diagnosis of Rare Diseases, Villa Sofia-Cervello Hospital, Palermo, Italy PubMed articlesGoogle scholar articles
  • Monica Cannata Department of Hematology for Rare Diseases of Blood and Blood-forming Organs, Laboratory for Molecular Diagnosis of Rare Diseases, Villa Sofia-Cervello Hospital, Palermo, Italy PubMed articlesGoogle scholar articles
  • Disma Renda Department of Hematology for Rare Diseases of Blood and Blood-forming Organs, Laboratory for Molecular Diagnosis of Rare Diseases, Villa Sofia-Cervello Hospital, Palermo, Italy PubMed articlesGoogle scholar articles
  • Giuseppina Calvaruso Department of Hematology for Rare Diseases of Blood and Blood-forming Organs, Laboratory for Molecular Diagnosis of Rare Diseases, Villa Sofia-Cervello Hospital, Palermo, Italy PubMed articlesGoogle scholar articles
  • Filippo Leto Department of Hematology for Rare Diseases of Blood and Blood-forming Organs, Laboratory for Molecular Diagnosis of Rare Diseases, Villa Sofia-Cervello Hospital, Palermo, Italy PubMed articlesGoogle scholar articles
  • Cristina Passarello Department of Hematology for Rare Diseases of Blood and Blood-forming Organs, Laboratory for Molecular Diagnosis of Rare Diseases, Villa Sofia-Cervello Hospital, Palermo, Italy PubMed articlesGoogle scholar articles
  • Aurelio Maggio Department of Hematology for Rare Diseases of Blood and Blood-forming Organs, Laboratory for Molecular Diagnosis of Rare Diseases, Villa Sofia-Cervello Hospital, Palermo, Italy PubMed articlesGoogle scholar articles
  • Antonino Giambona Department of Hematology for Rare Diseases of Blood and Blood-forming Organs, Laboratory for Molecular Diagnosis of Rare Diseases, Villa Sofia-Cervello Hospital, Palermo, Italy PubMed articlesGoogle scholar articles
  1. Correspondence to Dr Antonino Giambona, Department of Hematology for Rare Diseases of Blood and Blood-forming Organs, Laboratory for Molecular Diagnosis of Rare Diseases, Villa Sofia-Cervello Hospital, Palermo, Italy; a.giambona{at}villasofia.it
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Citation

Vinciguerra M, Cassarà F, Cannata M, et al
Phenotypic evaluations of HBB:c.93-23T>C, a nucleotide substitution in the IVS I nt 108 of β-globin gene
Journal of Clinical Pathology 2018;71:298-302.

Publication history

  • Received June 30, 2017
  • Revised July 14, 2017
  • Accepted July 19, 2017
  • First published August 9, 2017.
Online issue publication 
August 11, 2020

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© Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2018. All rights reserved. No commercial use is permitted unless otherwise expressly granted.