REFERENCES
- Liao C, Zhou JY, Xie XM, Li DZ. Screening for Hb Constant Spring in the Guangdong Province, South China, using the Sebia capillary electrophoresis system. Hemoglobin. 2011;35(1):87–90.
- Goossens M, Lee KY, Liebhaber SA, Kan YW. Globin structural mutant α125 Leu→Pro is a novel cause of α-thalassaemia. Nature. 1982;296(5860):864–865.
- Liang S, Wen XJ, Lin WX. Detection of the Hb Quong Sze mutation in a Chinese family by selective amplification of the α2-globin gene and restriction map analysis with Msp I. Hemoglobin. 1991;15(6):535–540.
- Chen FE, Ooi C, Ha SY, Genetic and clinical features of Hemoglobin H disease in Chinese patients. N Engl J Med. 2000;343(8):544–550.
- Munkongdee T, Pichanun D, Butthep P, Quantitative analysis of Hb Bart’s in cord blood by capillary electrophoresis system. Ann Hematol. 2011;90(7):741–746.
- Liao C, Zhou JY, Xie XM, Li J, Li R, Li D-Z. Detection of Hb Constant Spring by a capillary electrophoresis method. Hemoglobin. 2010;34(2):175–178.
- Chui DHK, Fucharoen S, Chan V. Hemoglobin H disease: not necessarily a benign disorder. Blood. 2003;101(3):791–800.
- Ma ES, Chan AY, Ha SY, Lau YL, Chan LC. Thalassemia screening based on red cell indices in the Chinese. Haematologica. 2001;86(12):1310–1311.
- Ma ESK, Chow EYD, Chan AYY, Chan LC. Interaction between (– –SEA) α-thalassemia deletion and uncommon nondeletional α-globin gene mutations in Chinese patients. Haematologica. 2001;86(5):539–540.