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Hemoglobin|January 1, 1979
Globin synthesis in bone marrow cells of patients with sickle cell anemia and beta O-thalassemia: contamination of the beta-chain with non-globin proteinsG Cividalli, H Kerem, E A RachmilewitzHemoglobin|May 24, 2011
Molecular lesion frequency of hemoglobin gene disorders in TaiwanSu-Ching Liu, Ching-Tien Peng, Tsai-Hsiu Lin, et al.Hemoglobin|May 24, 2011
Interactions of hydroxycarbamide (hydroxyurea) with iron and copper: implications on toxicity and therapeutic strategiesEleni Konstantinou, Ioannis Pashalidis, Annita Kolnagou, et al.Hemoglobin|May 24, 2011
The effect of the oral iron chelator deferiprone on the liver damage induced by tamoxifen in female ratsPavla Cerná, Dana Kotyzová, Vladislav EyblHemoglobin|December 23, 2011
Phenotype and genotype frequency of β-thalassemia and sickle cell disease carriers in Halkidiki, Northern GreeceChristoforos Kalleas, Kostas Anagnostopoulos, Klio Sinopoulou, et al.Hemoglobin|July 30, 2011
β-Thalassemia mutations found during 1 year of prenatal diagnoses in Fars Province, IranMohammad Saeid Rahiminejad, Sirous Zeinali, Abdolreza Afrasiabi, et al.Hemoglobin|July 30, 2011
A new α1-globin mutation, Hb Brugg [α20(B1)His→Gln]Mattia Rizzi, Karin Zurbriggen, Marlis Schmid, et al.Hemoglobin|July 30, 2011
Hb Extremadura [β64(E8)Gly→Ser;β133(H11)Val→Leu]: a new molecular analysisPaloma Ropero, Guillermo Martín-Nuñez, F A González, et al.Hemoglobin|July 30, 2011
A novel base change leading to Hb Vanderbilt [β89(F5)Ser→Arg, AGT>AGA]Matthew J Goodyer, Ezzat I Elhassadi, Melanie J Percy, et al.Pageof 238