http://orcid.org/0000-0002-1325-5489
References
- Flint J, Harding RM, Boyce AJ, et al. The population genetics of the haemoglobinopathies. Baillieres Clin Haematol. 1998;11(1):1–51.
- Fucharoen S, Ketvichit P, Pootrakul P, et al. Clinical manifestation of β-thalassemia/Hemoglobin E disease. J Pediatr Hematol Oncol. 2000;22(6):552–557.
- Fucharoen S, Winichagoon P. Clinical and hematologic aspects of Hemoglobin E β-thalassemia. Curr Opin Hematol. 2000;7(2):106–612.
- Winichagoon P, Fucharoen S, Chen P, et al. Genetic factors affecting clinical severity in β-thalassemia syndromes. J Pediatr Hematol Oncol. 2000;22(6):573–580.
- Nuinoon M, Makarasara W, Mushiroda T, et al. A genome-wide association identified the common genetic variants influence disease severity in β0-thalassemia/hemoglobin E. Hum Genet. 2010;127(3):303–314.
- Sripichai O, Munkongdee T, Kumkhaek C, et al. Coinheritance of the different copy numbers of α-globin gene modifies severity of β-thalassemia/Hb E disease. Ann Hematol. 2008;87(5):375–379.
- Pranee W, Vannarat S, Roongrat S, et al. Prenatal diagnosis of β-thalassaemia by reverse dot blot hybridization. Prenat Diagn 1999;19(5):428–435.
- Saechan V, Nopparatana C, Nopparatana C, et al. Molecular basis and hematological features of hemoglobin variants in Southern Thailand. Int J Hematol. 2010;92(3):445–450.
- 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.
- Fucharoen G, Fuchareon S, Jetsrisuparb A, et al. Eight-base deletion in exon 3 of the β-globin gene produced a novel variant (β khon kaen) with an inclusion body β-thalassemia trait. Blood 1991;78(2):537–539.
- Nuinoon M, Jeenduang N, Kesornsit A, et al. Hematological and molecular characterization of a novel Hb A2 variant with homozygous α-thalassemia-2 in a Southern Thai individual. Hemoglobin 2017;41(3):213–215.
- Chong SS, Boehm CD, Higgs DR, et al. Single-tube multiplex-PCR screen for common deletional determinants of α-thalassemia. Blood 2000;95(1):360–362.
- Fucharoen S, Shimizu K, Fukumaki Y. A novel C>T transition within the distal CCAAT motif of the Gγ-globin gene in the Japanese HPFH: implication of factor binding in elevated fetal globin expression. Nucl Acids Res. 1990;18(17):5245–5253.
- Kesornsit A, Jeenduang N, Horpet D, et al. Quantitative trait loci influencing Hb F levels in Southern Thai Hb E (HBB: c.79G>A) heterozygotes. Hemoglobin 2018;42(1):23–29.
- Amato A, Cappabianca MP, Perri M, et al. Hb Filottrano [codon 120 (–A)]: a novel frameshift mutation in exon 3 of the β-globin gene causing dominantly inherited β-thalassemia intermedia. Hemoglobin 2012;36(5):480–484.
- Kazazian HH, Jr, Dowling CE, Hurwitz RL, et al. Dominant thalassemia-like phenotypes associated with mutations in exon 3 of the β-globin gene. Blood 1992;79(11):3014–3018.
- Prehu C, Pissard S, Al-Sheikh M, et al. Two French Caucasian families with dominant thalassemia-like phenotypes due to hyper unstable hemoglobin variants: Hb Sainte Seve [codon 118 (–T)] and codon 127 [CAG→TAG (Gln→Stop]). Hemoglobin 2005;29(3):229–233.
- Fucharoen S, Kobayashi Y, Fucharoen G, et al. A single nucleotide deletion in codon 123 of the β-globin gene causes an inclusion body β-thalassaemia trait: a novel elongated globin chain β Makabe. Br J Haematol. 1990;75(3):393–399.
- Murru S, Loudianos G, Deiana M, et al. Molecular characterization of β-thalassemia intermedia in patients of Italian descent and identification of three novel β-thalassemia mutations. Blood 1991;77(6):1342–1347.
- Weinstein BI, Erramouspe B, Albuquerque DM, et al. Hb Florida: a novel elongated C-terminal β-globin variant causing dominant β-thalassemia phenotype. Am J Hematol. 2006;81(5):358–360.
- Delanoe-Garin J, Blouquit Y, Arous N, et al. Hemoglobin Saverne: a new variant with elongated β chains: structural and functional properties. Hemoglobin 1988;12(4):337–352.
- Ivaldi G, David O, Baffico M, et al. Hb Trento: an elongated C-terminal β chain due to a new frameshift mutation [β144 (–A)]. Hemoglobin 2003;27(1):15–25.