https://orcid.org/0000-0002-0399-0754
References
- Vrettou C, Traeger-Synodinos J, Tzetis M, et al. Rapid screening of multiple beta-globin gene mutations by real-time PCR on the LightCycler: application to carrier screening and prenatal diagnosis of thalassemia syndromes. Clin Chem. 2003;49(5):769–776.
- Muhammad R, Shakeel M, Rehman SU, et al. Population-based genetic study of β-thalassemia mutations in Mardan Division, Khyber Pakhtunkhwa Province, Pakistan. Hemoglobin. 2017;41(2):104–109.
- Sirichotiyakul S, Saetung R, Sanguansermsri T. Analysis of beta-thalassemia mutations in northern Thailand using an automated fluorescence DNA sequencing technique. Hemoglobin. 2003;27(2):89–95.
- Pornprasert S, Phusua A, Suanta S, et al. Detection of alpha-thalassemia-1 Southeast Asian type using real-time gap-PCR with SYBR Green1 and high resolution melting analysis. Eur J Haematol. 2008;80(6):510–514.
- Prathomtanapong P, Pornprasert S, Phusua A, et al. Detection and identification of beta-thalassemia 3.5 kb deletion by SYBR Green1 and high resolution melting analysis. Eur J Haematol. 2009;82(2):159–160.
- Shih HC, Er TK, Chang TJ, et al. Rapid identification of HBB gene mutations by high-resolution melting analysis. Clin Biochem. 2009;42(16–17):1667–1676.
- Bhardwaj U, Zhang YH, Lorey F, et al. Molecular genetic confirmatory testing from newborn screening samples for the common African-American, Asian Indian, Southeast Asian, and Chinese beta-thalassemia mutations. Am J Hematol. 2005;78(4):249–255.
- Saetung R, Ongchai S, Charoenkwan P, et al. Genotyping of beta thalassemia trait by high-resolution DNA melting analysis. Southeast Asian J Trop Med Public Health. 2013;44(6):1055–1064.
- Giardine B, Borg J, Viennas E, et al. Updates of the HbVar database of human hemoglobin variants and thalassemia mutations. Nucleic Acids Res. 2014;42(Database issue):D1063–D1069 (http://globin.cse.psu.eud).
- Hussain Z, Ansari S, Shamsi T. A perspective on thalassaemia. Natl j Health Sci. 2018;3(2):36–40.
- Ahmed S. Genetic haemoglobin disorders in Pakistan. Natl j Health Sci. 2017;2(3):95–99.
- Marashi SJ, Eshkoor SA, Saed Mirinargesi M, et al. Detection of eight common-globin gene mutation in thalassemia major patients using real time polymerase chain reaction (PCR)-high resolution melting and EvaGreen dye. Afr J Biotechnol. 2012;11(2):448–459.
- Islam MT, Sarkar SK, Sultana N, et al. High resolution melting curve analysis targeting the HBB gene mutational hot-spot offers a reliable screening approach for all common as well as most of the rare beta-globin gene mutations in Bangladesh. BMC Genet. 2018;19(1):1.
- Ramezanzadeh M, Salehi M, Salehi R. Assessment of high resolution melt analysis feasibility for evaluation of beta-globin gene mutations as a reproducible, cost-efficient and fast alternative to the present conventional method. Adv Biomed Res. 2016;5:71.