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Pediatric Hematology and Oncology Volume 22, 2005 - Issue 2
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HETEROZYGOUS β- THALASSEMIA AND HOMOZYGOUS H63D HEMOCHROMATOSIS IN A CHILD: An 18-Year Follow-Up

Roberto Miniero Department of Clinical and Biological Sciences, Department of Clinical and Biological Sciences, Orbassano (TO)Italy
, MD,
Irene Tardivo Department of Clinical and Biological Sciences, Department of Clinical and Biological Sciences, Orbassano (TO)Italy
, MD,
Antonella Roetto Department of Clinical and Biological Sciences, Department of Clinical and Biological Sciences, Orbassano (TO)Italy
, MD &
Marco De Gobbi Department of Clinical and Biological Sciences, Department of Clinical and Biological Sciences, Orbassano (TO)Italy
, MD
Pages 163-166 | Received 15 Mar 2004, Accepted 22 Oct 2004, Published online: 09 Jul 2009

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Herminio López-Escribano, Joana F. Ferragut, Maria M. Parera, Pilar Guix, José A. Castro, M. Misericòrdia Ramon & Antònia Picornell. (2012) Effect of Co-Inheritance of β-Thalassemia and Hemochromatosis Mutations on Iron Overload. Hemoglobin 36:1, pages 85-92.
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Articles from other publishers (2)

Thomas D. Coates. (2014) Physiology and pathophysiology of iron in hemoglobin-associated diseases. Free Radical Biology and Medicine 72, pages 23-40.
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I.F. Estevão, P. Peitl Junior & C.R. Bonini-Domingos. (2011) Serum ferritin and transferrin saturation levels in β0 and β+ thalassemia patients. Genetics and Molecular Research 10:2, pages 632-639.
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