References
- Itano HA. A third abnormal hemoglobin associated with hereditary hemolytic anemia. Proc Natl Acad Sci USA. 1951;37(12):775–784.
- Hardison RC, Chui DHK, Giardine B, et al. HbVar: a relational database of human hemoglobin variants and thalassemia mutations at the globin gene server. Hum Mutat. 2002;19(3):225–233. Available from: http://globin.cse.psu.edu
- Torres L. d S, Okumura JV, Silva D. G H d, et al. Hemoglobin D-Punjab: origin, distribution and laboratory diagnosis. Rev Bras Hematol Hemoter. 2015;37(2):120–126.
- Dass J, Gupta A, Mittal S, et al. Comparison of the characteristics of two hemoglobin variants, Hb D-Iran and Hb E, eluting in the Hb A2 window. Blood Res. 2017;52(2):130–134.
- Watson-Williams EJ, Beale D, Irvine D, et al. A A new haemoglobin, D-Ibadan (β-87 threonine–>lysine), producing no sickle-cell Haemoglobin D disease with Haemoglobin S. Nature. 1965;205:1273–1276.
- Bain BJ, Editor. Haemoglobinopathy Diagnosis. Malden (MA): Blackwell Science Inc.; 2002.
- Castro O, Winter WP, Bullock WH, et al. Hemoglobin D Ibadan trait in combination with βδ thalassemia. Hemoglobin. 1979;3(1):77–82.
- Lane PA, Witkowska HE, Falick AM, et al. Hemoglobin D Ibadan-β0 thalassemia: detection by neonatal screening and confirmation by electrospray-ionization mass spectrometry. Am J Hematol. 1993;44(3):158–161.
- Redding-Lallinger R, Tankut G, Holley L, et al. Molecular characterization of Hb D-Ibadan [β87(F3)Thr→Lys] in combination with Hb S [β6(A3)Glu→Val] and with β+–Thalassemia: report of two cases. Hemoglobin. 2002;26(2):129–134.
- Steinberg MH, Forget BG, Higgs DR, Nagel RL, Editors. Disorders of Hemoglobin Genetics, Pathophysiology and Clinical Management. Cambridge: Cambridge University Press; 2001.
- Falusi AG, Ogunmola GB, Esan GJ. Haemoglobin D-Ibadan in a Haemoglobin S endemic population. Afr J Med Med Sci. 1979;8(3–4):95–101.
- Huisman THJ. Combinations of β chain abnormal hemoglobins with each other or with β-thalassemia determinants with known mutations: influence on phenotype. Clin Chem. 1997;43(10):1850–1856.
- Rezende Pdo V, Costa Kda S, Domingues Junior JC, et al. Clinical, hematological and genetic data of a cohort of children with hemoglobin SD. Rev Bras Hematol Hemoter. 2016;38(3):240–246.
- Oberoi S, Das R, Trehan A, et al. HbSD-Punjab: clinical and hematological profile of a rare hemoglobinopathy. J Pediatr Hematol Oncol. 2014;36(3):e140–e144.
- Dolai T, Bera R, Maji S, et al. Profile of Hemoglobin D trait in West Bengal, India. Thalassemia Reports. 2014;4(1). Available from: http://www.pagepressjournals.org/index.php/thal/article/view/thal.2014.2152/5733.
- Gupta A, Saraf A, Dass J, et al. Compound heterozygous Hemoglobin D-Punjab/Hemoglobin D-Iran: a novel hemoglobinopathy. Indian J Hematol Blood Transfus. 2014;30(S1):409–412.
- Mutreja D, Tyagi S, Tejwani N, et al. Double heterozygous Hemoglobin Q India/Hemoglobin D Punjab hemoglobinopathy: report of two rare cases. Indian J Hum Genet. 2013;19(4):479–482.
- Hirsch RE, Witkowska HE, Shafer F, et al. HbC compound heterozygotes [HbC/Hb Riyadh and HbC/Hb N-Baltimore] with opposing effects upon HbC crystallization. Br J Haematol. 1997;97(2):259–265.
- Nagel RL, Lin MJ, Witkowska HE, et al. Compound heterozygosity for Hemoglobin C and Korle-Bu: moderate microcytic hemolytic anemia and acceleration of crystal formation [corrected]. Blood. 1993;82(6):1907–1912.
- Keren DF, Hedstrom D, Gulbranson R, et al. Comparison of Sebia Capillarys capillary electrophoresis with the Primus high-pressure liquid chromatography in the evaluation of hemoglobinopathies. Am J Clin Pathol. 2008;130(5):824–831.