References
- Higgs DR, Engel JD, Stamatoyannopoulos G. Thalassaemia. Lancet. 2011;379(9813):373–383
- Michelson AM, Orkin SH. Boundaries of gene conversion within the duplicated human α-globin genes. Concerted evolution by segmental recombination. J Biol Chem. 1983;258(24):15245–15254
- Goossens M, Dozy AM, Embury SH, et al. Triplicated α-globin loci in humans. Proc Natl Acad Sci USA. 1980;77(1):518–521
- Lie-Injo LE, Herrera AR, Kan YW. Two types of triplicated α-globin loci in humans. Nucleic Acids Res. 1981;9(15):3707–3717
- Wang W, Chan AY, Chan LC, et al. Unusual rearrangement of the α-globin gene cluster containing both the −α3.7 and αααanti 4.2 crossover junctions: Clinical diagnostic implications and possible mechanisms. Clin Chem. 2005;51(11):2167–2170
- Shang X, Li Q, Cai R, et al. Molecular characterization and clinical presentation of HKαα and anti-HKαα alleles in southern Chinese subjects.Clin Genet. 2013;83(5):472–476
- Hung CC, Lee CN, Chen CP, et al. Molecular assay of −α3.7 and −α4.2 deletions causing α-thalassemia by denaturing high-performance liquid chromatography. Clin Biochem. 2007;40(11):817–821
- Chong SS, Boehm CD, Higgs DR, Cutting GR. Single-tube multiplex-PCR screen for common deletional determinants of α-thalassemia. Blood. 2000;95(1):360–362
- Li D, Liao C, Li J, et al. Prenatal diagnosis of β-thalassemia in Southern China. Eur J Obstet Gynecol Reprod Biol. 2006;128(1–2):81–85
- Liao C, Li Q, Wei J, et al. Prenatal control of Hb Bart’s disease in southern China. Hemoglobin. 2007;31(4):471–475
- Xu XM, Zhou YQ, Luo GX, et al. The prevalence and spectrum of α- and β-thalassemia in Guangdong Province: Implications for the future health burden and population screening. J Clin Pathol. 2004;57(5):517–522
- Xiong F, Sun M, Zhang X, et al. Molecular epidemiological survey of hemoglobinopathies in the Guangxi Zhuang Autonomous Region of southern China. Clin Genet. 2010;78(2):139–148
- Fucharoen S, Viprakasit V. Hb H disease: Clinical course and disease modifiers. Hematology Am Soc Hematol Educ Program. 2009:26–34
- Chui DHK, Fucharoen S, Chan V. Hemoglobin H disease: Not necessarily a benign disorder. Blood. 2003;101(3):791–800
- Li Z, Cai S, Rong K, et al. The first compound heterozygosity for HKαα allele and Southeast Asian deletion allele. Clin Biochem. 2007;40(5–6):407–410