Diagnosis and molecular characterization of a novel α0 -thalassemia deletion (-Kozani ) found in a Greek child with unexplained microcytic hypochromic anemia-Reference-Cited by-同舟云学术

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

Published:2017-06-12 Issue:5 Volume:39 Page:e124-e126
ISSN:1751-5521
Container-title:International Journal of Laboratory Hematology
language:en
Short-container-title:Int J Lab Hem

Author:

Makis A.¹^ORCID,Georgiou I.²,Traeger-Synodinos J.³,Chaliasos N.¹,Grosso M.⁴,Gambale A.⁴,Iolascon A.⁴

Affiliation:

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

Publisher

Wiley

Subject

Biochemistry (medical),Clinical Biochemistry,Hematology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/ijlh.12690/fullpdf

Reference11 articles.

1. Microcytic anemia;DeLoughery;N Engl J Med,2014

2. How I Diagnose Non-thalassemic Microcytic Anemias;Bruno;Semin Hematol,2015

3. How I manage patients with atypical microcytic anaemia;Camaschella;Br J Haematol,2013

4. Beta-Thalassemia;Origa;Genet Med,2010

5. Phenotypic and molecular diversity of haemoglobin H disease: a Greek experience;Kanavakis;Br J Haematol,2000

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