https://orcid.org/0000-0002-8640-7375
References
- 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.
- Amrith M, Sobti PC. The burden of thalassemia in Punjab: a roadmap forward. J Pediatr Hematol Oncol. 2017;2(4):85–87.
- Lin M, Zhong TY, Chen YG, et al. Molecular epidemiological characterization and health burden of thalassemia in Jiangxi Province, P. R. China. PLoS One. 2014;9(7):e101505.
- He S, Qin Q, Yi S, et al. Prevalence and genetic analysis of α- and β-thalassemia in Baise region, a multi-ethnic region in southern China. Gene. 2017;619(1):71–75.
- Muncie HL, James C. α, and β thalassemia. AM Fam Physician. 2009;80(4):333–336.
- Passarello C, Giambona A, Cannata M, et al. Iron deficiency does not compromise the diagnosis of high HbA(2) thalassemia trait. Haematologica. 2012;97(3):472–473.
- Verhovsek M, So C-C, O'Shea T, et al. Is HbA2 level a reliable diagnostic measurement for β-thalassemia trait in people with iron deficiency? Am J Hematol. 2012;87(1):114–116.
- Pranpanus S, Sirichotiyakul S, Srisupundit K, et al. Sensitivity and specificity of mean corpuscular hemoglobin (MCH): for screening α-thalassemia-1 trait and β-thalassemia trait. J Med Assoc Thai. 2009;92(6):739–743.
- Sirichotiyakul S, Wanapirak C, Srisupundit K, et al. A comparison of the accuracy of the corpuscular fragility and mean corpuscular volume tests for the α-thalassemia 1 and β-thalassemia traits. Int J Gynaecol Obstet. 2009;107(1):26–29.
- Chan LC, Ma SK, Chan AYY, et al. Should we screen for globin gene mutations in blood samples with mean corpuscular volume (MCV) greater than 80 fL in areas with a high prevalence of thalassaemia? J Clin Pathol. 2001;54(4):317–320.
- Liao C, Li DZ, Li J. First detection of the codons 41-43 (–CTTTG,+A) β-thalassemia mutation in a Chinese patient. Ann Hematol. 2008;87(9):775–776.