References
- World population data sheet. Population Reference Bureau, Washington, DC, 2012. (http://www.prb.org/pdf12/2012-population-data-sheet_eng.pdf)
- Black ML, Wang W, Bittles AH. Unity and diversity: Genetic studies on the population of China. In: Santos C, Lima M, Eds. Recent Advances in Molecular Biology and Evolution: Applications to Biological Anthropology. Trivandrum, Kerala: Research Signpost. 2007:347–371
- Bittles AH. Endogamy, consanguinity and community genetics. J Genet. 2002;81(3):91–98
- Census of India (2001–2003) Report on Causes of Death, Office of Registrar General, India. (http://www.censusindia.gov.in/Vital_Statistics/Summary_Report_Death_01_03.pdf, p 2.)
- Weatherall DJ, Clegg JB. Inherited haemoglobin disorders: An increasing global health problem. Bull World Health Organ. 2001;79(8):704–712
- Christianson A, Howson CP, Modell B. March of Dimes global report on birth defects. March of Dimes Birth Defects Foundation, White Plains. 2006:24–27
- World Health Organization: Guidelines for the control of haemoglobin disorders. In: Modell B, Ed. Report of the VIth Annual Meeting of the WHO Working Group on Haemoglobinopathies held in Cagliari, Sardinia, 8–9 April 1989
- Management of Haemoglobin Disorders. Report of a Joint WHO-TIF (Thalassaemia International Federation) Meeting held at Nicosia, Cyprus, 16–18 November 2007. WHO Library Cataloguing-in-Publication Data. Geneva, Switzerland: printed by the WHO Production Services. (NLM classification: WH 190)
- World population data sheet. Population Reference Bureau, Washington, DC, 2009. (http://www.prb.org/pdf09/09wpds_eng.pdf)
- 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
- Agarwal MB, Mehta BC. Genotypic analysis of symptomatic thalassaemia syndromes (a study of 292 unrelated cases from Bombay). J Postgrad Med. 1982;28(1):1–3
- Thalassaemia and other haemoglobinopathies. World Health Organization Resolutions, May 2006, EB118.R1 and WHA59.20. (http://www.who.int/gb/ebwha/pdf_files/EBSS-EB118-2005-REC1/english/Res/res-eb118_2006_rec1-en.pdf.)
- Das SK, Madhusnata DE, Bhattacharya DK, et al. Interaction of different hemoglobinopathies in Eastern India with a view to establish genotype-phenotype correlation. Am J Hum Biol. 2000;12(4):452–459
- Kukreti R, Dash D, Vineetha KE, et al. Spectrum of β-thalassemia mutations and their association with allelic sequence polymorphisms at the β-globin gene cluster in an Eastern Indian population. Am J Hematol. 2002;70(4):269–277
- Bandyopadhyay A, Bandyopadhyay S, Basak J, et al. Profile of β-thalassemia in eastern India and its prenatal diagnosis. Prenat Diagn. 2004;24(12):992–996
- Census 2011 (http://www.censusindia.gov.in/2011-prov-results/data_files/west%20bengal/1-at_a_glance_wb.xls)
- Fuchareon S, Winichagoon P. Hemoglobinopathies in Southeast Asia. Hemoglobin. 1987;11(1):65–88
- Na-Nakorn S, Wasi P. The distribution of Haemoglobin E: Haemoglobin E triangle in Southeast Asia. J Med Assoc Thai. 1972;61(1):65–68
- Ong-Ajyooth S, Suthipark K, Shumnumsirivath D, et al. Oxidative stress and antioxidants in β thalassaemia/Haemoglobin E. J Med Assoc Thai. 1987;70(5):270–274