References
- Wang W, Kham SK, Yeo GH, et al. Multiplex minisequencing screen for common Southeast Asian and Indian β-thalassemia mutations. Clin Chem. 2003;49(2):209–218
- Weatherall DJ, Clegg JB. The Thalassaemia Syndromes, 4th ed. Oxford, UK: Blackwell Science, 2001
- Weatherall DJ. The global problem of genetic disease. Ann Hum Biol. 2005;32(2):117–122
- Ng IS, Ong JB, Tan CL, Law HY. β-Thalassemia mutations in Singapore – A strategy for prenatal diagnosis. Hum Genet. 1994;94(4):385–388
- Xu X, Liao C, Liu Z, et al. Antenatal screening and fetal diagnosis of β-thalassemia in a Chinese population: Prevalence of the β-thalassemia trait in the Guangzhou area of China. Hum Genet. 1996;98(2):199–202
- Haj Khelil A, Perrin P, Lefranc G, Ben Chibani J. Synthetic review on the different anthropological aspects of hemoglobinopathies in Tunisia. Int J Mod Anthrop. 2012;5(1):60–78
- Chan OT, Westover KD, Dietz L, et al. Comprehensive and efficient HBB mutation analysis for detection of β-hemoglobinopathies in a pan-ethnic population. Am J Clin Pathol. 2010;133(5):700–707
- Olivieri NF. The β-Thalassemias. N Engl J Med. 1999;341(2):99–109
- Old JM, Petrou M, Modell B, Weatherall DJ. Feasibility of antenatal diagnosis of β thalassaemia by DNA polymorphisms in Asian Indian and Cypriot populations. Br J Haematol. 1984;57(2):255–263
- Cai SP, Zhang JZ, Huang DH, et al. A simple approach to prenatal diagnosis of β-thalassemia in a geographic area where multiple mutations occur. Blood. 1988;71(5):1357–1360
- Stoming TA, Diaz-Chico JC, Yang KG, et al. Newer developments in the identification of β-thalassemia. Hemoglobin. 1988;12(5–6):565–576
- Cai SP, Kan YW. Identification of the multiple β-thalassemia mutations by denaturing gradient gel electrophoresis. J Clin Invest. 1990;85(2):550–553
- Losekoot M, Fodde R, Harteveld CL, et al. Denaturing gradient gel electrophoresis and direct sequencing of PCR amplified genomic DNA: A rapid and reliable diagnostic approach to β thalassaemia. Br J Haematol. 1990;76(2):269–274
- Sutcharitchan P, Saiki R, Fucharoen S, et al. Reverse dot-blot detection of Thai β-thalassaemia mutations. Br J Haematol. 1995;90(4):809–816
- Sutcharitchan P, Saiki R, Huisman THJ, et al. Reverse dot-blot detection of the African-American β-thalassemia mutations. Blood. 1995;86(4):1580–1585
- Wong C, Dowling CE, Saiki RK, et al. Characterization of β-thalassaemia mutations using direct genomic sequencing of amplified single copy DNA. Nature. 1987;330(6146):384–386
- Old JM, Varawalla NY, Weatherall DJ. Rapid detection and prenatal diagnosis of β-thalassaemia: Studies in Indian and Cypriot populations in the UK. Lancet. 1990;336(8719):834–837
- Atanasovska B, Bozhinovski G, Plaseska-Karanfilska D, Chakalova L. Efficient detection of Mediterranean β-thalassemia mutations by multiplex single-nucleotide primer extension. PLoS One. 2012;7(10):e48167. doi: 10.1371/journal.pone.0048167
- Pastinen T, Partanen J, Syvanen AC. Multiplex, fluorescent, solid-phase minisequencing for efficient screening of DNA sequence variation. Clin Chem. 1996;42(9):1391–1397
- Fiorentino F, Magli MC, Podini D, et al. The minisequencing method: An alternative strategy for preimplantation genetic diagnosis of single gene disorders. Mol Hum Reprod. 2003;9(7):399–410
- Kerkeni E, Monastiri K, Saket B, et al. Association among education level, occupation status, and consanguinity in Tunisia and Croatia. Croat Med J. 2006;47(4):656–661
- Fattoum S. Hemoglobinopathies in Tunisia. An updated review of the epidemiologic and molecular data. Tunis Med. 2006;84(11):687–696
- Haj Khelil A, Denden S, Leban N. Hemoglobinopathies in North Africa: A review. Hemoglobin. 2010;34(1):1–23
- Ben Charfeddine I, Riepe FG, Clauser E, et al. Steroid 21-hydroxylase gene mutational spectrum in 50 Tunisian patients: Characterization of three novel polymorphisms. Gene. 2012;507(1):20–26