REFERENCES
- Kollias G, Wrighton N, Hurst J, Grosveld F. Regulated expression of Aγ- β-, and hybrid γβ-globin genes in transgenic mice: manipulation of the developmental expression patterns. Cell 1986; 46(1)89–94
- Weatherall DJ. The phenotypic diversity of monogenic disease: lessons from the thalassaemias. Harvey Lectures 1998–1999; 94: 1–20
- Bouva M, Harteveld CL, van Delft P, Giordano PC. Known and new δ globin gene mutations and their diagnostic significance. Haematologica 1006; 91(1)129–132
- Stamatoyannopoulos G, Nienhuis AW. Hemoglobin switching. The Molecular Basis of Blood Diseases 2nd, G Stamatoyannopoulos, AW Nienhuis, PW Majerus, H Varmus. W.B. Saunders Company, Philadelphia 1994; 135–182
- Wood WG. Increased Hb F in adult life. Bailliere's Clin Haematol 1993; 6: 177–213
- Bollekens JA, Forget BG. δβ Thalassemia and hereditary persistence of fetal hemoglobin. Hematol Oncol Clin North Am 1991; 5(3)399–422
- Najmabadi H, Karimi-Nejad R, Sahebjam S, Pourfarzad F, Teimourian S, Sahebjam F, Amirizadeh N, Karimi-Nejad MH. The β-thalassemia mutation spectrum in the Iranian population. Hemoglobin 2001; 25(3)285–296
- Yavarian M, Harteveld CL, Batelaan D, Bernini LF, Giordano PC. Molecular spectrum of β-thalassemia in the Iranian province of Hormozgan. Hemoglobin 2001; 25(1)35–43
- Galanello R, Borgna-Pignatti C. Prevention of thalassaemias and other haemoglobin disorders. TIF Publication 2003; 1: 56
- Miller SA, Dykes DD, Polesky HF. A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res 1988; 16(3)1215
- Betke K, Marti HR, Schlicht I. Estimation of small percentages of foetal haemoglobin. Nature 1959; 184(Suppl 24)1877–1878
- Craig JE, Barnetson RA, Prior J, Raven JL, Thein SL. Rapid detection of deletions causing δβ thalassemia and hereditary persistence of fetal hemoglobin by enzymatic amplification. Blood 1994; 83(6)1673–1682
- http://globin.bx.psu.edu/hbvar/menu.html
- Hardison RC, Chui DHK, giardine B, Riemer C, Patrinos GP, Anagnou n, Miller W, Wajcman H. HbVar: a relational database of human hemoglobin variants and thalassemia mutations at the globin gene server. Hum Mutat 2002; 19(3):225–233 (http://globin.cse.psu.edu).
- Feingold EA, Forget BG. The breakpoint of a large deletion causing hereditary persistence of fetal hemoglobin occurs within an erythroid DNA domain remote from the β-globin gene cluster. Blood 1989; 74(6)2178–2186
- Zertal-Zidani S, Ducrocq R, Weil-Olivier C, Elion J, Krishnamoorthy R. A novel δβ fusion gene expresses Hemoglobin A (Hb A) not Hb Lepore: Senegalese δ0β+-thalassemia. Blood 2001; 98(4)1261–1263
- Camaschella C, Serra A, Saglio G, Baiget M, Magaretti N, Mantovani R, Ottolenghi S. The 3′ ends of the deletions of Spanish δβ0-thalassemia and Black HPFH 1 and HPFH 2 lie within 17 kilobases. Blood 1987; 70(2)593–596
- Najmabadi H, Ghamari A, Sahebjam F, Kariminejad R, Hadavi V, Khatibi T, Samavat A, Mehdipour E, Modell B, Kariminejad MH. Fourteen-year experience of prenatal diagnosis of thalassaemia in Iran. Commun Genet 2006; 9(2)93–97
- Harteveld CL, Voskamp A, Phylipsen M, Akkermans N, den Dunnen JT, White SJ, Giordano PC. Nine unknown rearrangements in 16p13.3 and 11p15.4 causing α- and β-thalassaemia characterised by high resolution multiplex ligation-dependent probe amplification. J Med Genet 2005; 42(12)922–931