https://orcid.org/0000-0002-4597-6272
References
- Weatherall DJ. The inherited diseases of hemoglobin are an emerging global health burden. Blood. 2010;115(22):4331–4336.
- Singh N, Hira JK, Chhabra S, et al. Misdiagnosis of double heterozygous εGγ(Aγδβ)0-thalassemia/β++ thalassemia as homozygous β-thalassemia: a pitfall for molecular diagnostic laboratories. Blood Cells Mol Dis. 2020;81:102394.
- Yilmaz Keskin E, Acar Ö, Özbas H. Missed diagnosis of β-thalassemia trait in premarital screening due to accompanying HbA2-Yialousa (HBD: c.82G>T). J Pediatr Hematol Oncol. 2021;43(1):e103–e104.
- Fucharoen G, Sanchaisuriya K, Sae-Ung N, et al. A simplified screening strategy for thalassaemia and haemoglobin E in rural communities in south-east Asia. Bull World Health Organ. 2004;82(5):364–372.
- Brancaleoni V, Di Pierro E, Motta I, et al. Laboratory diagnosis of thalassemia. Int J Lab Hem. 2016;38(Suppl 1):32–40.
- Joutovsky A, Hadzi-Nesic J, Nardi MA. HPLC retention time as a diagnostic tool for hemoglobin variants and hemoglobinopathies: a study of 60000 samples in a clinical diagnostic laboratory. Clin Chem. 2004;50(10):1736–1747.
- Srivorakun H, Singha K, Fucharoen G, et al. A large cohort of hemoglobin variants in Thailand: molecular epidemiological study and diagnostic consideration. PLoS One. 2014;9(9):e108365.
- Tan AS, Quah TC, Low PS, et al. A rapid and reliable 7-deletion multiplex polymerase chain reaction assay for alpha-thalassemia. Blood. 2001;98(1):250–251.
- Winichagoon P, Saechan V, Sripanich R, et al. Prenatal diagnosis of beta-thalassaemia by reverse dot-blot hybridization. Prenat Diagn. 1999;19(5):428–435.
- Viprakasit V, Chinchang W. Two independent origins of Hb Dhonburi (Neapolis) [beta 126 (H4) Val->Gly]: an electrophoretically silent hemoglobin variant. Clin Chim Acta. 2007;376(1-2):179–183.
- Pagano L, Viola A, Fioretti G, et al. Neapolis (CD 126 beta+ GGT->GGG): a result of a screening in Campania, a region in Southern Italy. Haematologica. 2007;92(7):990–991.
- Bardakdjian-Michau J, Fucharoen S, Delanoe-Garin J, et al. Hemoglobin Dhonburi alpha 2 beta 2 126 (H4) Val––Gly: a new unstable beta variant producing a beta-thalassemia intermedia phenotype in association with beta zero-thalassemia. Am J Hematol. 1990;35(2):96–99.