References
- Weatherall D J, Clegg J B. Hereditary persistence of fetal hemoglobin. In: Gibbons R, Higgs D R, Olivieri N F, Wood W F, Eds. The Thalassaemia Syndromes. 4th ed. Oxford: Blackwell Scientific Publishers, 2001:450–455.
- Weatherall D J. The thalassemia. In: Stamatoyannopoulos G, Majerus P W, Perlmutter R M, Varmus H E, Eds. The Molecular Basis of Blood Diseases. 4th ed. Philadelphia: WB Saunders Company, 2001:135–182.
- Pirastu M, Ristaldi M S, Loudianos G, Murru S, Sciarratta G V, Parodi M I, Leone D, Agosti S, Cao A. Molecular analysis of atypical β-thalassemia heterozygotes. Ann NY Acad Sci 1990; 612:90–97, [PUBMED], [INFOTRIEVE]
- Trifillis P, Ioannou P, Schwartz E, Surrey S. Identification of four novel δ-globin gene mutations in Greek Cypriots using polymerase chain reaction and automated fluorescence-based DNA sequence analysis. Blood 1991; 78(12):3298–3305, [PUBMED], [INFOTRIEVE], [CSA]
- Samavat A, Modell B. Iranian national thalassaemia screening program. BMJ 2004; 329(7475):1134–1137, [PUBMED], [INFOTRIEVE], [CROSSREF], [CSA]
- Old J M, Varawalla N Y, Weatherall D J. Rapid detection and prenatal diagnosis of β-thalassaemia: studies in Indian and Cypriot populations in the UK. Lancet 1990; 33(8719):834–837, [CROSSREF], [CSA]
- Tzetis M, Traeger-Synodinos J, Kanavakis E, Metaxotou-Mavromati A, Kattamis C. The molecular basis of normal Hb A2 (type 2) β-thalassemia in Greece. Hematol Pathol 1994; 8(1–2):25–34, [PUBMED], [INFOTRIEVE], [CSA]
- De Angioletti M, Lacerra G, Gaudiano C, Mastrolonardo G, Pagano L, Mastrullo L, Masciandaro S, Carestia C. Epidemiology of the δ globin alleles in southern Italy shows complex molecular, genetic, and phenotypic features. Hum Mutat 2002; 20(5):358–367, [PUBMED], [INFOTRIEVE], [CROSSREF], [CSA]
- Dedoussis G V, Mandilara G D, Boussiu M, Loutradis A. Hb F production in β thalassemia heterozygotes for the IVS-II-1 G→A β0-globin mutation. Implication of the haplotype and the Gγ − 158 C→T mutation on the Hb F level. Am J Hematol 2000; 64(3):151–155, [PUBMED], [INFOTRIEVE], [CROSSREF], [CSA]
- Yavarian M, Karimi M, Bakker E, Harteveld C L, Giordano P C. Response to hydroxyurea treatment in Iranian transfusion-dependent β-thalassemia patients. Haematologica 2004; 89(10):1172–1178, [PUBMED], [INFOTRIEVE], [CSA]
- Karimi M, Yarmohammadi H, Farjadian S, Zeinali S, Moghaddam Z, Cappellini M D, Giordano P C. β-Thalassemia intermedia from southern Iran: IVS-II-1 (G→A) is the prevalent thalassemia intermedia allele. Hemoglobin 2002; 26(2):147–154, [PUBMED], [INFOTRIEVE], [CROSSREF], [CSA]