References
- Clarke G M, Higgins T N. Laboratory investigation of hemoglobinopathies and thalassemias: review and update. Clin Chem 2000; 46(8, Pt. 2)1284–1290
- Old J M. Screening and genetic diagnosis of haemoglobin disorders. Blood Rev 2003; 17(1)43–53
- Najmabadi H, Karimi‐Nejad R, Sahebjam S, Pourfarzad F, Teimourian S, Sahebjam F, Amirizadeh N, Karimi‐Nejad M H. The β‐thalassemia mutation spectrum in the Iranian population. Hemoglobin 2001; 25(3)285–296
- Najmabadi H, Pourfathollah A A, Neishabury M, Sahebjam F, Krugluger W, Oberkanins C. Rare and unexpected mutations among Iranian β‐thalassemia patients and prenatal samples discovered by reverse‐hybridization and DNA sequencing. Haematologica 2002; 87(10)1113–1114
- Neishabury M, Oberkanins C, Moheb L A, Pourfathollah A A, Kahrizi K, Keyhany E, Krugluger W, Najmabadi H. High prevalence of the − α3.7 deletion among thalassemia patients in Iran. Hemoglobin 2003; 27(1)53–55
- Garshasbi M, Oberkanins C, Law H Y, Neishabury M, Kariminejad R, Najmabadi H. α‐Globin gene deletion and point mutation analysis among in Iranian patients with microcytic hypochromic anemia. Haematologica 2003; 88(10)1196–1197
- Bardakdjian‐Michau J, Fucharoen S, Delanoe‐Garin J, Kister J, Lacombe C, Winichagoon P, Blouquit Y, Riou J, Wasi P, Galacteros F. Hemoglobin Dhonburi α2β2126(H4)Val→Gly: a new unstable β variant producing a β‐thalassemia intermedia phenotype in association with β0‐thalassemia. Am J Hematol 1990; 35(2)96–99
- Pagano L, Lacerra G, Camardella L, De Angioletti M, Fioretti G, Maglione G, de Bonis C, Guarino E, Viola A, Cutolo R, De Rosa L, Carestia C. Hemoglobin Neapolis, β126(H4)Val→Gly: a novel β‐chain variant associated with a mild β‐thalassemia phenotype and displaying anomalous stability features. Blood 1991; 78(11)3070–3075
- Pagano L, Carbone V, Fioretti G, Viola A, Buffardi S, Rametta V, Desicato S, Pucci P, De Rosa C. Compound heterozygosity for Hb Lepore‐Boston and Hb Neapolis (Dhonburi) [β126(H4)Val→Gly] in a patient from Naples, Italy. Hemoglobin 1997; 21(1)1–15
- Huisman T HJ, Carver M FH, Baysal E. A Syllabus of Thalassemia Mutations (1997). The Sickle Cell Anemia Foundation, Augusta 1997