REFERENCES
- Verma IC. The challenge of genetic disorders in India. Proceedings of the First Annual Ranbaxy Science Foundation Symposium held at New Dehli, India, September 1994. 1994:11–20.
- Verma IC, Choudhry VP, Jain PK. Prevention of thalassemia: a necessity in India. Indian J Pediatr. 1992;59(6):649–654.
- Giardine B, van Baal S, Kaimakis P, . HbVar database of human hemoglobin variants and thalassemia mutations: 2007 update. Hum Mutat. 2007;28(2):206.
- Clarke GM, Higgins TN. Laboratory investigation of hemoglobinopathies and thalassemias: review and update. Clin Chem. 2000;46(8B):1284–1290.
- Rund D, Cohen T, Filon D, . Evolution of a genetic disease in an ethnic isolate: β-thalassemia in the Jews of Kurdistan. Proc Natl Acad Sci USA. 1991;88(1):310–314.
- Sinha S, Black ML, Agarwal S, . Profiling β-thalassaemia mutations in India at state and regional levels: implications for genetic education, screening and counselling programmes. Hugo J. 2009;3(1–4):51–62.
- Colah R, Gorakshakar A, Nadkarni A, . Regional heterogeneity of β-thalassemia mutations in the multi ethnic Indian population. Blood Cells Mol Dis. 2009;42(3):241–246.
- Nadkarni A, Gorakshakar A, Surve R, . Hematological and molecular analysis of novel and rare β-thalassemia mutations in the Indian population. Hemoglobin. 2009;33(1):59–65.
- Edison ES, Shaji RV, Devi SG, . Analysis of β globin mutations in the Indian population: presence of rare and novel mutations and region-wise heterogeneity. Clin Genet. 2008;73(4):331–337.
- Chakrabarti P, Gupta R, Mishra A, Rai M, Singh VP, Dash D. Spectrum of β-thalassemia mutations in North Indian states: a β-thalassemia trait with two mutations in cis. Clin Biochem. 2005;38(6):576–578.
- Pawar AR, Colah RB, Mohanty D. A novel β+-thalassemia mutation (codon 10 GCC→GCA) and a rare transcriptional mutation (−28 A→G) in Indians. Blood. 1997;89(10):3888–3894.
- Bhat VS, Dewan KK, Krishnaswamy PR, Mandal AK, Balaram P. Characterization of a hemoglobin variant : HbQ-India/IVS-I-1 [G>T] β-thalassemia. Ind J Clin Biochem. 2010;25(1):99–104.
- Mandal AK, Bisht S, Bhat VS, Krishnaswamy PR, Balaram P. Electrospray mass spectrometric characterization of Hemoglobin Q (Hb Q-India) and a double mutant Hemoglobin S/D in clinical samples. Clin Biochem. 2008;41(8):75–81.
- Bashyam MD, Bashyam L, Savithri GR, Gopikrishna M, Sangal V, Devi AR. Molecular genetic analyses of β-thalassemia in South India reveals rare mutations in the β-globin gene. J Hum Genet. 2004; 49(8):408–413.
- Varawalla NY, Old JM, Weatherall DJ. Rare β-thalassaemia mutations in Asian Indians. Br J Haematol. 1991;79(4):640–644.
- Huang S, Zeng F, Chen M, . The δ-globin RNA transcript level in β-thalassemia carriers. Acta Hematologica 1999;102(1):1–6.
- Perseu L, Satta S, Moi P, . R. KLF1 gene mutations cause borderline Hb A2. Blood. 2011;118(16):4454–4458.
- El-Agouza I, Abu Shahla A, Sirdah M. The effect of iron deficiency anaemia on the levels of haemoglobin subtypes: possible consequences for clinical diagnosis. Clin Lab Haematol. 2002;24(5):285–289.
- Kulkarni GD, Kulkarni SS, Kadakol GS, . Molecular basis of β-thalassemia in Karnataka, India. Genet Test Mol Biomarkers. 2012;16(2):138–141.
- Shaji RV, Edison, ES, Poonkuzhali B, Srivastava A, Chandy M. Rapid Detection of β-globin gene mutations and polymorphisms by temporal temperature gradient gel electrophoresis. Clin Chem. 2003;49(5):777–781.
- Prins J, van der Meijden, BB, Blokland EAW, Wielders, JPM, Kraaijenhagen, RJ. Hemoglobin disorders detected in diabetic patients by Hb A1c analysis. Ned Tijdschr Klin Chem Labgeneesk. 2005;30(4):298–299.
- Nasir NM, Thevarajah M, Yean CY. Hemoglobin variants detected by hemoglobin A1c (Hb A1c) analysis and the effects on Hb A1c measurements. Int J Diabetes Dev Ctries. 2010;30(2):86–90.