References
- Xu XM, Zhou YQ, Luo GX, et al. 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
- Xiong F, Sun M, Zhang X, et al. Molecular epidemiological survey of haemoglobinopathies in the Guangxi Zhuang Autonomous Region of southern China. Clin Genet. 2010;78(2):139–148
- Yang Y, Li DZ. A survey of pregnancies with Hb Bart’s disease in Mainland China. Hemoglobin. 2009;33(2):132–136
- Li DZ, Li J, Liao C. Prenatal diagnosis of Hemoglobin Bart’s disease caused by co-inheritance of two different α0-thalassemia defects in China. Prenat Diagn. 2009;29(6):632–633
- Liu YT, Old JM, Miles K, et al. Rapid detection of α thalassaemia deletions and α-globin gene triplication by multiplex polymerase chain reactions. Br J Haematol. 2000;108(2):295–299
- Liao C, Wei J, Li Q, et al. Nonimmune hydrops fetalis diagnosed during the second half of pregnancy in Southern China. Fetal Diagn Ther. 2007;22(4):302–305
- Liao C, Li Q, Wei J, et al. Prenatal control of Hb Bart’s disease in southern China. Hemoglobin. 2007;31(4):471–475
- Higgs DR, Ayyub H, Chong SS. The – –THAI and – –FIL determinants of α-thalassemia in Taiwan. Am J Hematol. 1999;60(1):80–81
- Tang HS, Zhou JY, Xie XM, Li DZ. Newborn screening for α-thalassaemia by a capillary electrophoresis method. J Med Screen. 2012;19(3):159
- Li X, Zhou Q, Zhang M, et al. Sonographic markers of fetal α-thalassemia major. J Ultrasound Med. 2015;34(2):197–206
- Tongsong T, Wanapirak C, Sirivatanapa P, et al. Prenatal eradication of Hb Bart’s hydrops fetalis. J Reprod Med. 2001;46(1):18–22
- Leung KY, Liao C, Li QM, et al. A new strategy for prenatal diagnosis of homozygous α0-thalassemia. Ultrasound Obstet Gynecol. 2006;28(2):173–177