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Clinical and molecular characterization of novel deletions causing epsilon gamma delta beta thalassemia: Report of two cases

  • Published:2019-10 Issue:10 Volume:215 Page:152578
  • ISSN:0344-0338
  • Container-title:Pathology - Research and Practice
  • language:en
  • Short-container-title:Pathology - Research and Practice

Author:

Repnikova Elena,Roberts Jennifer,Mc Dermott Sarah,Farooqi Midhat S,Iqbal Nazia Tabassum,Silvey Michael,Nolen JDL,Taboada Eugenio,Li Weijie

Publisher

Elsevier BV

Subject

Cell Biology,Pathology and Forensic Medicine

Reference11 articles.

1. Identification and molecular characterization of a novel 163 kb deletion: the Italian (εγδβ)(0)-thalassemia;Cardiero;Hematology.,2016

2. First report of a novel deletion due to εγδβ–thalassemia in a Chinese family;Hui;Hemoglobin.,2017

3. Blueberry muffin skin lesions in an infant with epsilon gamma Delta Beta thalassemia;Puar;Pediatr. Dev. Pathol.,2019

4. Anemia in children: prevalence, causes, diagnostic work-up, and long-term consequences;Allali;Expert Rev. Hematol.,2017

5. Thrombocytopenia and platelet transfusion in the neonate;Cremer;Semin. Fetal Neonatal Med.,2016

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