References
- Kukreti R, Rao B C, Das S K, De M, Talukder G, Vaz F, Verma I C, Brahmachari S K. Study of the single nucleotide polymorphism (SNP) at the palindromic sequence of hypersensitive site (HS-4) of the human β-globin locus control region (LCR) in Indian population. Am J Hematol 2002; 69(1):77–79, [PUBMED], [INFOTRIEVE], [CSA]
- Kukreti R, Dash D, Chakrabarty S, Das S K, De M, Talukder G. Spectrum of β thalassemia mutations and their association with allelic sequence polymorphism of the β globin gene cluster in an Eastern Indian population. Am J Hematol 2002; 70(4):269–277, [PUBMED], [INFOTRIEVE], [CROSSREF], [CSA]
- Chakrabarti S, Sengupta B, De M, Talukder G. Presence of an extremely rare β-thalassemia mutation in a couple referred for prenatal diagnosis. A case report. J Vivekananda Inst Med Sci 2002; 25(1):27–29, [CSA]
- Gajra B, Bandyopadhyay D, Chakrabarti S, Sengupta B, De M, Shaji R V, Talukder G. Thalassemia β0 due to identical frameshift mutation codon 15 (− T) in both parents. Am J Hematol 2004; 75(2):117, [PUBMED], [INFOTRIEVE], [CROSSREF], [CSA]
- Chakrabarti S, De M, Das S K, Das N, Bhattacharya D K, Talukder G. Screening for haemoglobin variants by molecular study in tribal populations of Tripura. Nucleus 1996; 39(3):148–150, [CSA]
- De M, Das S K, Bhattacharya D K, Talukder G. The occurence of β-thalassemia mutation and its interaction with Hemoglobin E in the Eastern India. Int J Hematol 1997; 66(1):31–34, [PUBMED], [INFOTRIEVE], [CROSSREF], [CSA]
- De M, Chakrabarty G, Das S K, Bhattacharya D K, Talukder G. Molecular studies of Haemoglobin E in tribal populations of Tripura. Lancet 1997; 349(9061):1297, [PUBMED], [INFOTRIEVE], [CROSSREF], [CSA]
- Das S K, Talukder G. A review on the origin and spread of deleterious mutants of the β-globin gene in Indian population. Homo 2001; 52(2):93–109, [PUBMED], [INFOTRIEVE], [CROSSREF], [CSA]
- Fodde R, Losekoot M, van den Broek M H, Oldenburg M, Rashida N, Schreuder A, Wijnen J T, Giordano P C, Nayudu N V, Khan P M. Prevalence and heterogeneityof α+ thalassemia in two tribal populations from Andhra Pradesh, India. Hum Genet 1998; 80(2):157–160, [CROSSREF], [CSA]
- Fodde R, Harteveld C L, Losekoot M, Giordano P C, Khan P M, Nayudu N V, Bernini L F. Multiple recombination events are responsible for the heterogeneity of α+ thalassemia haplotypes among the forest tribes of Andhra Pradesh, India. Ann Hum Genet 1991; 55(Pt 1):43–50, [PUBMED], [INFOTRIEVE], [CSA]
- Reddy P H, Modell B. Reproductive behaviour and natural selection for the sickle gene in the Baiga tribe of central India. The role of social parenting. Ann Hum Genet 1996; 60(Pt 3):231–236, [PUBMED], [INFOTRIEVE], [CSA]
- Adhikari D, Lahiri P, Chandra S, Bhattacharya D K. A method for estimating Haemoglobins A2 and E for mass detection of carriers of thalassemia. Curr Sci 1987; 56(24):1281–1283, [CSA]
- Betke K, Marti H R, Schlicht I. Estimation of small percentages of foetal haemoglobin. Nature 1959; 184(Suppl 24):1877–1878, [PUBMED], [INFOTRIEVE], [CSA]
- Newton C R, Graham A, Heptinstall L E, Powell S J, Sunmmers C, Kalsheker N, Smith J C, Markham A F. Analysis of any point mutation in DNA. The amplification refractory mutation system (ARMS). Nucleic Acids Res 1989; 17(7):2503–2516, [PUBMED], [INFOTRIEVE], [CSA]
- Shaji R V, Srivastava A, Chandy M, Krishnamoorthy R. A single tube multiplex PCR method to detect the common α+-thalassemia alleles. Blood 2000; 95(5):1879–1880, [PUBMED], [INFOTRIEVE], [CSA]
- Bittles A H. Genomics and the changing profile of human disease. Biol Int 2003; 45:3–8, [CSA]
- Bhasin M K, Bhasin V. Ecology people and health. In: Bhasin M K, Malik S L, eds. The Indian Scenario in Anthropology Trends and Applications. Delhi: Kamla Raj, 2002:1–23.
- Giri A K, Datta S, Gajra B, Raychaudhury A, Talukder G, Sharma A. Relative frequency of some genetic markers in tribal and nontribal populations from the Midnapore district, West Bengal. J Cytol Genet 1981; 16(1):179–184, [CSA]
- Sengupta B, Chakrabarti S, Gajra B, De M, Bhattacharya D K, Talukder G. Study of E β thalassemia in Eastern India (West Bengal). Poster Presentation at the 4th HUGO Pacific Meeting of the 5th Asia Pacific Conference on Human Genetics, Ambassador City Jomtien, CholburiThailand, October 27–30, 2002.
- Das S K, De M, Bhattacharya D K, Talukder G. Molecular characterization of hereditary persistence of foetal haemoglobin mutation by restriction fragment length polymorphism mapping. Cytobios (USA) 2001; 106(Suppl 2):229–232, [CSA]
- Gajra B, Sengupta B, Chakrabarti S, Talukder G. Abnormal haemoglobin mutants in populations of India—possible index of environmental pollution. Poster Presentation at the XXVIII Annual Conference and Special Symposium on Arsenic Contamination Ground Water and Its Health Effects, CalcuttaIndia, February 14–16, 2003.