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Hemoglobin
international journal for hemoglobin research
Volume 37, 2013 - Issue 1
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Short Communication

Homozygosity for the Severe β+-Thalassemia Mutation [IVS-I-5 (G>C)] Causes the Phenotype of Thalassemia Trait: An Extremely Rare Presentation

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Pages 101-105 | Received 30 May 2012, Accepted 02 Oct 2012, Published online: 12 Dec 2012

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