References
- Colah RB, Gorakshakar AC, Nadkarni AH. Invasive & non-invasive approaches for prenatal diagnosis of haemoglobinopathies: Experiences from India. Indian J Med Res. 2011;134:552–560
- Ramani KV, Mavalankar DV, Govil D. Study of blood-transfusion services in Maharashtra and Gujarat States, India. J Health Popul Nutr. 2009;27(2):259–270
- Thacker N. Prevention of thalassemia in India. Indian Pediatr. 2007;44(9):647–648
- Patrinos GP, Giardine B, Riemer C, et al. Improvements in the HbVar database of human hemoglobin variants and thalassemia mutations for population and sequence variation studies. Nucleic Acids Res. 2004;32(Database issue):D537–D541 (http://globin.cse.psu.edu)
- Patel AP, Naik MR, Shah NM, et al. Prevalence of common hemoglobinopathies in Gujarat: An analysis of a large population screening program. Nat J Community Med. 2012;3(1):112–116
- Stephens AD, Angastiniotis M, Baysal E, et al. International council for the standardisation of haematology (ICSH). ICSH recommendations for the measurement of Haemoglobin A2. Int J Lab Hematol. 2012;34(1):1–13
- Rangan A, Sharma P, Dadu T, et al. β-Thalassemia mutations in subjects with borderline Hb A2 values: A pilot study in North India. Clin Chem Lab Med. 2011;49(12):2069–2072
- Mayuranathan T, Rayabaram J, Edison ES, et al. A novel deletion of β-globin promoter causing high Hb A2 in an Indian population. Haematologica. 2012;97(9):1445–1447
- Higgs DR, Thein SL, Wood WG. Distribution and population genetics of the thalassaemias. In: Weatherall DJ, Clegg JB, Eds. The Thalassaemia Syndromes, 4th ed. Oxford, UK: Blackwell Science. 2001:237–286
- Sheth JJ, Sheth FJ, Pandya P, et al. β-Thalassemia mutations in western India. Indian J Pediatr. 2008;75(6):567–570
- Vaz FE, Chakur CB, Banerjee MK, et al. Distribution of β-thalassemia mutations in the Indian population referred to a diagnostic center. Hemoglobin. 2000;24(3):181–194
- Kumar R, Singh K, Panigrahi I, et al. Genetic heterogeneity of β globin mutations among Asian-Indians and importance in genetic counselling and diagnosis. Mediterr J Hematol Infect Dis. 2013;5(1):1–5
- Kulkarni GD, Kulkarni SS, Kadakol GS, et al. Molecular basis of β-thalassemia in Karnataka, India. Genet Test Mol Biomarkers. 2012;16(2):138–141
- Adekile AD, Kazanetz EG, Leonova JY, et al. Co-inheritance of Hb D-Punjab (codon 121; GAA → CAA) and β0-thalassemia (IVS-II-1; G → A). J Pediatr Hematol Oncol. 1996;18(2):151–153
- Ostrowsky JT, Lippman A, Scriver CR. Cost-benefit analysis of a thalassemia disease prevention program. Am J Public Health. 1985;75(7):732–736