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Vinaykumar Bohara, Lalit Raut, Girish Badarkhe, Siddartha S. Roy & Utpal Chaudhuri. (2013) Homozygosity for the Severe β+-Thalassemia Mutation [IVS-I-5 (G>C)] Causes the Phenotype of Thalassemia Trait: An Extremely Rare Presentation. Hemoglobin 37:1, pages 101-105.
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Mehdi Haghi, Abbas A. Hosseinpour Feizi, Cornelis L. Harteveld, Nasser Pouladi & Mohammad A. Hosseinpour Feizi. (2009) Homozygosity for a Rare β0-Thalassemia Mutation [Frameshift Codons 25/26 (+T)] Causes β-Thalassemia Intermedia in an Iranian Family. Hemoglobin 33:1, pages 75-80.
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Articles from other publishers (2)
R. Angalena, K. N. Prabitha, A. K. Chaudhary, M. D. Bashyam, S. Jain & A. B. Dalal. (2010) LETTER TO THE EDITOR: A novel homozygous point mutation at codon 82 (HBB:c.247A > T) in the beta‐globin gene leads to thalassemia major. International Journal of Laboratory Hematology 32:5, pages 548-549.
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Francesca Salvatori, Giulia Breveglieri, Cristina Zuccato, Alessia Finotti, Nicoletta Bianchi, Monica Borgatti, Giordana Feriotto, Federica Destro, Alessandro Canella, Eleonora Brognara, Ilaria Lampronti, Laura Breda, Stefano Rivella & Roberto Gambari. (2009)
Production of β‐globin and adult hemoglobin following G418 treatment of erythroid precursor cells from homozygous β
0
39 thalassemia patients
. American Journal of Hematology 84:11, pages 720-728.
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