References
- Baysal E. HPFH and db-thalassemia conditions. Hemoglobin. 1993;17:569–589. doi: https://doi.org/10.3109/03630269309043499
- Weatherall DJ, Clegg JB. The thalassemia syndromes. 3rd ed. Oxford: Blackwell Scientific Publications; 1981. p. 875.
- Lim WF, Muniandi L, George E, et al. Hbf in HbE/β-thalassemia. a clinical and laboratory correlation. Hematology. 2015;20(6):349–353. doi: https://doi.org/10.1179/1607845414Y.0000000203
- Higgs DR, Thein SL, Wood WG, editors. The molecular pathology of the thalassemias. The thalassemia syndromes. 4th ed. Oxford: Blackwell Science; 2001, p. 133–191.
- Balgir RS. The burden of haemoglobinopathies in India and the challenges ahead. Curr Sci. 2000;79(11):1536–15347.
- Thein SL, Weatherall DJ. A non-deletion hereditary persistence of fetal hemoglobin (HPFH) determinant not linked to the beta-globin gene complex. Prog Clin Biol Res. 1989;316B:97–111.
- Nadkarni A, Wadia M, Gorakshakar A, et al. Molecular characterization of δβ-thalassemia and hereditary persistence of fetal haemoglobin in the Indian population. Haemoglobin. 2008;32(5):425–433. doi: https://doi.org/10.1080/03630260802341687
- Bollekens JA, Forget BC. Thalassemia and hereditary persistence of fetal hemoglobin. Hematol Oncol Clin North Am. 1991;5:399–422.
- Craig JE, Barnetson RA, Prior J, et al. Rapid detection of deletions causing delta beta thalassemia and hereditary persistence of fetal hemoglobin by enzymatic amplification. Blood. 1994;83(6):1673–1682.
- Baysal E, Huisman TH. Detection of common deletional alphathalassemia-2 determinants by PCR. Am J Hematol. 1994;46:208–213. doi: https://doi.org/10.1002/ajh.2830460309
- Smetanina NS, Huisman TH. Detection of alpha-thalassemia-2 (−3.7 kb) and its corresponding triplication ααα (anti-3.7 kb) by PCR: an improved technical change. Am J Hematol. 1996;53:202–203. doi: https://doi.org/10.1002/(SICI)1096-8652(199611)53:3<202::AID-AJH11>3.0.CO;2-F
- Chang JG, Lee LS, Lin CP, et al. Rapid diagnosis of alpha thalassemia-1 of Southeast Asia type and hydrops fetailis by polymerase chain reaction. Blood. 1991;78:853–854.
- Shaji RV, Eunice SE, Baidya S, et al. Determination of the breakpoint and molecular diagnosis of a common alpha-thalassaemia-1 deletion in the Indian population. Br J Haematol. 2003;123:942–947. doi: https://doi.org/10.1046/j.1365-141.2003.04704.x
- Wood WG. Hereditary persistence of fetal hemoglobin and δβ-thalassemia. In: Steinberg MH, Forget BG, Higgs DR, Nagel RL, editor. Disorders of hemoglobin: genetics, pathophysiology, and clinical management. Cambridge: Cambridge University Press; 2001. p. 356–388.
- Mayuranathan T, Rayabaram J, Das R, et al. Identification of rare and novel deletions that cause (δβ)0-thalassaemia and hereditary persistence of foetal haemoglobin in Indian population. Eur J Haematol. 2014;92(6):514–520. doi: https://doi.org/10.1111/ejh.12276
- Forget BG. Molecular basis of hereditary persistence of fetal hemoglobin. Ann NY Acad Sci. 1998;850:38–44. doi: https://doi.org/10.1111/j.1749-6632.1998.tb10460.x
- Khunger JM, Gupta M, Singh R, et al. Haematological characterisation and molecular basis of Asian Indian inversion deletions delta beta thalassemia: a case report. J Clin Diagn Res. 2014 Sep;8(9):FD01–FD02.
- Supan F, Yutthana P, Satja S, et al. Molecular and hematological characterization of hereditary persistence of fetal hemoglobin-6/ Indian deletion – inversion Gγ(Aγδβ)0-thalassemia and Gγ(Aγδβ)0-thalassemia/HbE in Thai patients. Am J Hematol. 2002;71:109–113. doi: https://doi.org/10.1002/ajh.10202
- Carrocini GCS, Ondei LS, Zamaro PJA, et al. Evaluation of HPFH and δβ-thalassemia mutations in a Brazilian group with high Hb F levels. Mol Res. 2011;10(4):3213–3219. doi: https://doi.org/10.4238/2011.December.21.3
- Ottolenghi S, Giglioni B, Taramelli R, et al. Molecular comparison of δβ thalassemia and hereditary persistence of fetal hemoglobin DNAs: evidence of a regulatory area? Proc Natl Acad Sci USA. 1982;79(7):2347–2351. doi: https://doi.org/10.1073/pnas.79.7.2347
- Galanello R, Cao A. Relationship between genotype and phenotype; thalassemia intermedia. Ann NY Acad Sci. 1998;850(850):325–333. doi: https://doi.org/10.1111/j.1749-6632.1998.tb10489.x
- Tan Jin Ai MA, Yap SF, Tan KL, et al. Mild beta-thalassemia intermedia caused by compound heterozygosity for G(A)o/-thalassemia and molecular characterization of the defect in four Chinese families. Acta Haematol. 2003;109(4):169–175. doi: https://doi.org/10.1159/000070965
- Pandey S, Pandey S, Ranjan R, et al. Phenotypic heterogeneity of Asian Indian inversion deletions Gγ(aγδβ)0 breakpoint A and breakpoint B. Ind J Clin Biochem. 2013;28(1):98–101. doi: https://doi.org/10.1007/s12291-012-0232-9