Citations (63)
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T. P. Molchanova & T. H. J. Huisman. (1997) The Levels of Abnormal Hemoglobin in Persons with Heterozygosities for an a Chain Variant and for β-Thalassemia. Hemoglobin 21:2, pages 173-177.
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T. H. J. Huisman. (1997) Hb E and α-Thalassemia; Variability in the Assembly of βE Chain Containing Tetramers. Hemoglobin 21:3, pages 227-236.
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S. A. Liebhaber. (1989) α Thalassemia. Hemoglobin 13:7-8, pages 685-731.
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B. L. Anderson Fernandes. (1989) HB N-Baltimore or β95(FG2)LYS→GLU in Portugal. Hemoglobin 13:1, pages 83-87.
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L. N. Shulman & H. F. Bunn. (1988) Hb Deer Lodge in a Caucasian American: Effect of Iron Deficiency on Level of Variant. Hemoglobin 12:2, pages 197-199.
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S. Rahbar, G. Nozari, R. Chillar & R. Bruce Wallace. (1988) Further Evidence for a Post-Translational Phenomenon in the Interaction of α-Thalassemia with Sickle Cell Trait. Hemoglobin 12:1, pages 71-76.
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G. Martinez, R. Ferreira, A. Hernandez, A. Di Rienzo & B. Colombo. (1986) Association of HB H Disease with Sickle-Trait. Hemoglobin 10:4, pages 421-425.
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K. D. Lanclos, A. Kutlar, F. Kutlar, P. J. Ojwang, A. L. Reese & T. H. J. Huisman. (1986) The Effect of α-Thalassemia on the Level of Hybrid Hemoglobin Variants in Heterozygotes. Hemoglobin 10:4, pages 401-416.
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Samir K. Ballas & Deborah K. Park. (1985) Biosynthetic Evidence for Stability of Hb N-Baltimore. Hemoglobin 9:5, pages 489-494.
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K. C. Carstairs, A. Raulfs, A. Kutlar, S. S. Chen, B. B. Webber, J. B. Wilson & T. H. J. Huisman. (1985) Hb Fort Worth Or α227 (B8)Glu→Glyβ2 in a Black Family from Canada. Hemoglobin 9:2, pages 201-205.
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M. B. Gardiner, J. Carver, B. L. Abraham, J. B. Wilson & T. H. J. Huisman. (1982) Further Studies on the Quantitation of the Hemoglobins A, S, C, and F in Newborn Babies with Difffrent Hemoglobinopathies Using High Pressure Liquid Chromatography. Hemoglobin 6:1, pages 1-13.
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. (1981) Binding of βs, βC and βO Arab Globins to the Erythrocyte Membrane. Hemoglobin 5:5, pages 501-505.
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. (1981) The First Homozygote for the Hereditary Persistence of Fetal Hemoglobin Observed in the Southeastern United States. Hemoglobin 5:4, pages 411-416.
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Wanda J. Whitten & Donald L. Rucknagel. (1981) The Proportion of HB A2 is Higher in Sickle Cell Trait Than in Normal Homozygotes. Hemoglobin 5:4, pages 371-378.
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S. Musumeci, G. Schiliro, A. Fisher, A. Musco, M. Maritiucci, F. Mavilio, P. P. Fontanarosa & L. Tentori. (1979) Hb J Baltimore (β 16 (A13) Gly ↣ Asp) in Association with β-Thalassemia in a Sicilian Family. Hemoglobin 3:6, pages 459-464.
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G. Brittenham, B. Lozoff, J. W. Harris, N. V. S. Nayudu, M. Gravely, J. B. Wilson, H. Lam & T. H. J. Huisman. (1978) Hemoglobin Hofu or αβ [126 (H4) Val → Glu] Found in Combination with Hemoglobin S. Hemoglobin 2:6, pages 541-549.
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E. P. Orringer, A. Felice, A. Reese, J. B. Wilson, H. Lam, M. E. Gravely & T. H. J. Huisman. (1978) Hb Nottingham (α;2β;2 (FG5) 98 VAL→GLY) in a Caucasian Male: Clinical and Biosynthetic Studies. Hemoglobin 2:4, pages 315-332.
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Articles from other publishers (43)
Catherine M. Tucker & Douglas F. Stickle. (2023) Quantitation of hemoglobins using Sebia Capillarys-2 capillary electrophoresis (CE) for A1c: Comparison to results using CE for hemoglobins. Practical Laboratory Medicine 34, pages e00312.
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Thais Helena Chaves Batista, Marcondes José de Vasconcelos Costa Sobreira, Rodrigo Marcionilo de Santana, Gabriela da Silva Arcanjo, Camila Mabel de Albuquerque Ramos, Dulcinéia Martins Albuquerque, Aderson da Silva Araujo, Ana Cláudia Mendeonça dos Anjos, Fernando Ferreira Costa, Antonio Roberto Lucena-Araujo & Marcos André Cavalcanti Bezerra. (2019) Interaction between hemoglobin S and N-Baltimore: a case report in Pernambuco, Brazil. Hematology, Transfusion and Cell Therapy 41:4, pages 365-368.
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Diego Velasco-Rodríguez, Juan-Manuel Alonso-Domínguez, Fernando-Ataúlfo González-Fernández, Alfonso Muriel, Lorena Abalo, María Sopeña, Jesús Villarrubia, Paloma Ropero, María Paz Plaza, María Tenorio, Ana Jiménez-Martín, Gemma Moreno, Jorge Martínez-Nieto, Félix de la Fuente-Gonzalo, Marina Fernández-Escribano, Francisco Javier López-Jiménez & Fernando Cava. (2016) Laboratory parameters provided by Advia 2120 analyser identify structural haemoglobinopathy carriers and discriminate between Hb S trait and Hb C trait. Journal of Clinical Pathology 69:10, pages 912-920.
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$${\text{[}}\beta _{\text{2}} {\text{(A4)Glu}} \to {\text{Gly}}\alpha _{\text{2}} {\text{],}}$$
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2
β
2
131
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