A Novel εγδβ-Thalassemia Deletion Associated with Severe Anemia at Birth and a β-Thalassemia Intermedia Phenotype Later in Life in Three Generations of a Greek Family-Reference-Cited by-同舟云学术

A Novel εγδβ-Thalassemia Deletion Associated with Severe Anemia at Birth and a β-Thalassemia Intermedia Phenotype Later in Life in Three Generations of a Greek Family

Published:2019-12-12 Issue: Volume: Page:1-4
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Makis Alexandros¹^ORCID,Georgiou Ioannis²,Traeger-Synodinos Jan³^ORCID,Storino Maria Rosaria⁴,Giuliano Mariarosaria⁴,Andolfo Immacolata⁴,Hatzimichael Eleftheria⁵,Chaliasos Nikolaos¹,Giapros Vasileios⁶,Izzo Paola⁴,Iolascon Achille⁴,Grosso Michela⁴

Affiliation:

1. Department of Pediatrics, Faculty of Medicine, University of Ioannina, Ioannina, Greece;

2. Genetics and In Vitro Fertilization Unit, Department of Obstetrics and Gynecology, Faculty of Medicine, University of Ioannina, Ioannina, Greece;

3. Laboratory of Medical Genetics, National and Kapodistrian University of Athens, Athens, Greece;

4. Department of Molecular Medicine and Medical Biotechnology, CEINGE, Advanced Biotechnologies, University of Naples Federico II, Naples, Italy;

5. Department of Hematology, Faculty of Medicine, University of Ioannina, Ioannina, Greece;

6. Neonatal Intensive Care Unit, Faculty of Medicine, University of Ioannina, Ioannina, Greece

Publisher

Informa UK Limited

Subject

Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology

Link

https://www.tandfonline.com/doi/pdf/10.1080/03630269.2019.1699568

Reference16 articles.

1. Beta-thalassemia

2. The Molecular Basis of -Thalassemia

3. A novel epsilon gamma delta beta thalassemia presenting with pregnancy complications and severe neonatal anemia

4. First Report of a Novel Deletion Due toεγδβ-Thalassemia in a Chinese Family

5. Gamma-Beta Thalassemia: A Cause of Hemolytic Disease of the Newborn

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