References
- Shang X, Peng Z, Ye Y, et al. Rapid targeted next-generation sequencing platform for molecular screening and clinical genotyping in subjects with hemoglobinopathies. EBioMedicine. 2017;23:150–159.
- He S, Zhang Q, Li D, et al. Prevention and control of Hb Bart’s disease in Guangxi Zhuang Autonomous Region, China. Eur J Obstet Gynecol Reprod Biol. 2014;178:138–141.
- Taher AT, Weatherall DJ, Cappellini MD. Thalassaemia. Lancet. 2018;391(10116):155–167.
- Li J, Li R, Zhou J-Y, et al. Prenatal control of nondeletional α thalassemia: first experience in mainland China. Prenat Diagn. 2013;33(9):869–872.
- Tang W, Zhang C, Lu F, et al. Spectrum of α-thalassemia and β-thalassemia mutations in the Guilin Region of southern China. Clin Biochem. 2015;48(16–17):1068–1072.
- Long J, Yan S, Lao K, et al. The diagnosis and molecular analysis of a novel 21.9 kb deletion (Qinzhou type deletion) causing α+ thalassemia. Blood Cells Mol Dis. 2014;52(4):225–229.
- Li D, Liao C, Li J, et al. Detection of alpha-thalassemia in beta-thalassemia carriers and prevention of Hb Bart’s hydrops fetalis through prenatal screening. Haematologica. 2006;91(5):649–651.
- Zertal-Zidani S, Ducrocq R, Weil-Olivier C, et al. A novel delta beta fusion gene expresses hemoglobin A (HbA) not Hb Lepore: Senegalese delta(0)beta(+) thalassemia. Blood. 2001;98(4):1261–1263.
- Lou J-W, He Y, Liu Y-H, et al. Detection of Hb anti-Lepore Hong Kong (NG_000007.3: g.63154_70565dup) in Chinese individuals. Hemoglobin. 2014;38(2):146–148.
- So C-C, Chan AYY, Tsang STY, et al. A novel beta-delta globin gene fusion, anti-Lepore Hong Kong, leads to overexpression of delta globin chain and a mild thalassaemia intermedia phenotype when co-inherited with beta(0)-thalassaemia. Br J Haematol. 2007;136(1):158–162.
- Stephens AD, Angastiniotis M, Baysal E, et al. ICSH recommendations for the measurement of haemoglobin A2. Int J Lab Hematol. 2012;34(1):1–13.
- Cui J, Azimi M, Hoppe CC. Detection of a novel βδ-globin fusion gene, Anti-Lepore Hb CHORI (βthrough IVS-I-57/δfrom IVS-I-101), by multiplex ligation-dependent probe amplification. Hemoglobin. 2014;38(1):60–63.
- Long J, Liu E. The carriage rates of αααanti3.7, αααanti4.2, and HKαα in the population of Guangxi, China measured using a rapid detection qPCR system to determine CNV in the α-globin gene cluster. Gene. 2021;768:145296.