Diagnosis and molecular characterization of a novel α0 -thalassemia deletion (-Kozani) found in a Greek child with unexplained microcytic hypochromic anemia

Diagnosis and molecular characterization of a novel α⁰ -thalassemia deletion (-Kozani) found in a Greek child with unexplained microcytic hypochromic anemia

Int J Lab Hematol. 2017 Oct;39(5):e124-e126. doi: 10.1111/ijlh.12690. Epub 2017 Jun 12.

¹ Child Health Department, Faculty of Medicine, University of Ioannina, Ioannina, Greece.
² Genetics and IVF 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, University of Naples Federico II, CEINGE- Advanced Biotechnologies, Italy.

No abstract available