REFERENCES
- Li J, Xie XM, Zhou JY, Li DZ. Co-inheritance of β- and δ-thalassemia compromising prenatal screening in a Chinese couple seeking prevention. Fetal Diagn Ther. 2011;30(1):73–76.
- Xu XM, Zhou YQ, Luo GX, . The prevalence and spectrum of α and β thalassaemia in Guangdong Province: implications for the future health burden and population screening. J Clin Pathol. 2004; 57(5):517–522.
- Matsuda M, Sakamoto N, Fukumaki Y. δ-Thalassemia caused by disruption of the site for an erythroid-specific transcription factor, GATA-1, in the δ-globin gene promoter. Blood. 1992;80(5):1347–1351.
- Huang CH, Ko TM, Chiang YL, Lin CS. Mutation at −30 (T→C) of the δ-globin gene in a Taiwanese β-thalassemia carrier. Hemoglobin. 2003;27(3):205–209.
- 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.
- Frischknecht H, Troxler H, Dutly F, . Characterization of three novel δ chain hemoglobin variants and two δ-thalassemia alleles. Hemoglobin. 2012;34(4):374–382.
- Qin WB, Ju TL, Yue XL, . Hb A2-Liangcheng [γ117(G19)Asn→Asp(AAC→GAC)]: a new δ chain variant detected by gene analysis in a Chinese family. Hemoglobin. 1993;17(5):463–466.
- Sharma RS, Williams L, Wilson JB, Huisman THJ. Hemoglobin-A2-Coburg or α2δ2116Arg→His (G18). Biochim Biophys Acta. 1975;393(2):379–382.
- Codrington JF, Kutlar F, Harris HF, Wilson JB, Stoming TA, Huisman THJ. Hb A2-Wrens or α2δ298(FG5)Val→Met, an unstable δ chain variant identified by sequence analysis of amplified DNA. Biochim Biophys Acta. 1989;1009(1):87–89.
- Moi P, Paglietti E, Sanna A, . Delineation of the molecular basis of δ- and normal Hb A2 β-thalassemia. Blood. 1988;72(2):530–533.
- Trifillis P, Kyrri A, Kalogirou E, . Analysis of δ-globin gene mutations in Greek Cypriots. Blood. 1993;82(5):1647–1651.
- Moo-Penn WF, McPhedran P, Bobrow S, Johnson MH, Jue DL, Olsen KW. Hemoglobin Connecticut (β21(B3)Asp→Gly): a hemoglobin variant with low oxygen affinity. Am J Hematol. 1981; 11(2):137–145.
- Sansone G, Carrell RW, Lehmann H. Haemoglobin Genova: β-28 (B10) leucine→proline. Nature. 1967;214(5091):877–879.
- Hopmeier P, Binder C, Gadner H, Fischer M. A case of the unstable Hb Genova (β28 Leu→Pro) in an Arab child associated with severe haemolytic anaemia and growth retardation. Acta Haematol. 1990; 83(1):39–34.
- Keeling MM, Ogden LL, Wrightstone RN, . Hemoglobin Louisville (β42 (CD1) Phe→Leu): an unstable variant causing mild hemolytic anemia. J Clin Invest. 1971;50(11):2395–2402.
- Adams JG 3rd, Morrison WT, Barlow RL, Steinberg MH. Hb Mississippi [β44(CD3)Ser→Arg]: a new variant with anomalous properties. Hemoglobin. 1987;11(5):435–452.
- Imamura T, Fujita S, Ohta Y, Hanada M, Yanase T. Hemoglobin Yoshizuka (G10(108)β asparagine→aspartic acid): a new variant with a reduced oxygen affinity from a Japanese family. J Clin Invest. 1969;48(12):2341–2348.
- Morga do A, Picanço I, Gomes S, . Mutational spectrum of δ-globin gene in the Portuguese population. Eur J Haematol. 2007;79(5):422–428.
- Pavlou E, Phylactides M, Kyrri A, . δ-Thalassemia in Cyprus. Hemoglobin. 2006;30(4):455–462.
- De Angioletti M, Lacerra G, Gaudiano C, . Epidemiology of the δ globin alleles in southern Italy shows complex molecular, genetic, and phenotypic features. Hum Mutat. 2002;20(5):358–367.
- Bennani M, Mombo LE, Chaventre A, . Origin of Hb A2′ (Hb B2) [δ16(A13)Gly→Arg (GGC→CGC)]. Hemoglobin. 2003;27(2):105–110.
- Spurdle AB, Krause A, Ramsay M, Jenkins T. The high frequency of the Hb B2 variant in the Herero population: a founder effect? Hemoglobin. 1994;18(4–5):317–323.