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Case Reports in Hematology
Volume 2017, Article ID 9265396, 3 pages
https://doi.org/10.1155/2017/9265396
Case Report

HbS-Sicilian (δβ)0-Thalassemia: A Rare Variant of Sickle Cell

Cleveland Clinic Lerner College of Medicine (CCLCM), Case Western University, 9500 Euclid Avenue, Cleveland, OH 44195, USA

Correspondence should be addressed to Grace Onimoe; gro.fcc@geomino

Received 24 April 2017; Revised 3 August 2017; Accepted 17 August 2017; Published 17 September 2017

Academic Editor: Neelam Giri

Copyright © 2017 Grace Onimoe and Genine Smarzo. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

How to Cite this Article

Grace Onimoe and Genine Smarzo, “HbS-Sicilian (δβ)0-Thalassemia: A Rare Variant of Sickle Cell,” Case Reports in Hematology, vol. 2017, Article ID 9265396, 3 pages, 2017. https://doi.org/10.1155/2017/9265396.