REFERENCES
- Weatherall DJ, Clegg JB. The Thalassaemia Syndromes, 4th ed. Oxford: Blackwell Science, 2001.
- Pirastu M, Galanello R, Melis MA, δ+-Thalassemia in Sardinia. Blood. 1983;62(2):341–345.
- Ohta Y, Yamaoka K, Sumida I, Fujita S, Fujimura T,Yanase T. Homozygous δ-thalassemia first discovered in a Japanese family with hereditary persistence of fetal hemoglobin. Blood. 1971;37(6):706–715.
- Ohta Y, Yasukawa M, Saito S, Fujita S, Kobayashi Y. Homozygous δ thalassemia in Japan. Hemoglobin. 1980;4(3–4):417–425.
- Eram SM, Azimifar B, Abolghassemi H, The IVS-II-I (G→A) β0-thalassemia mutation in cis with Hb A2-Troodos [δ116(G18)Arg→Cys (CGC→TGC)] causes a complex prenatal diagnosis in a Iranian family. Hemoglobin. 2005;29(4):289–292.
- Zeinali S, Eram SM, Azimifar B, Lotfi V, Fouladi P, Masrouri M. First report on co-inheritance of (β) IVS-I-I (G→T) thalassemia with the (γ) CD85 [Phe→Ser (F1) (TTT→TCT)] Hb A2 Etolia in Iran. Hematologica. 2006;91:(6)45–46.
- Huisman THJ, Jonxis JHP. The Hemoglobinopathies Techniques of Identification. Clinical and Biochemical Analysis, Vol. 6. New York: Marcel Dekker Inc., 1977.
- Miller SA, Dykes DD, Polesky HF. A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acid Res. 1988;16(3):1215.
- Ko TM, Tseng LH, Hsieh FJ, Hsu PM, Lee TY. Carrier detection and prenatal diagnosis of α thalassemia of Southeast Asian deletion by polymerase chain reaction. Hum Genet. 1992;88(3): 245–248.
- Trifillis P, Loannou 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.
- Trifillis P, Kurri A, Kalogirou E, Analysis of δ-globin mutations in Greek Cypriots. Blood. 2009;82(5):1647–1651.