References
- Modell B, Darlison M. Global epidemiology of haemoglobin disorders and derived service indicators. Bull World Health Organ. 2008;86(6):480–487.
- Patrinos GP, Giardine B, Riemer C, et al. Improvements in the HbVar database of human hemoglobin variants and thalassemia mutations for population and sequence variation studies. Nucleic Acids Res. 2004;32(Database issue):D537–D541 (http://globin.cse.psu.edu/).
- Thom CS, Dickson CF, Gell DA, et al. Hemoglobin variants: biochemical properties and clinical correlates. Cold Spring Harb Perspect Med. 2013;3(3):a011858.
- Mantikou E, Arkesteijn SG, Beckhoven van JM, et al. A brief review on newborn screening methods for hemoglobinopathies and preliminary results selecting β thalassemia carriers at birth by quantitative estimation of the HbA fraction. Clin Biochem. 2009;42(18):1780–1785.
- Oliveira JL, Swanson K, Wendt P, et al. Hb Cambridge-MA [β144(HC1)-β146(HC3)Lys-Tyr-His→0 (HBB c.433 A>T)]: a new high oxygen affinity variant. Hemoglobin 2010;34(6):565–571.
- Kent WJ, Sugnet CW, Furey TS, et al. The human genome browser at UCSC. Genome Res. 2002;12(6):996–1006. http://genome.ucsc.edu/).
- Bunn HF. Forget BG. Hemoglobin: Molecular, Genetic, and Clinical Aspects. Philadelphia (PA, USA): W.B. Saunders Company, 1986.
- Mrad A, Blouquit Y, Lacombe C, et al. Hb Tunis [alpha 2 beta 2 124 (H2)Pro. Hemoglobin 1988;12(1):23–30.
- Bursaux E, Blouquit Y, Poyart C, et al. Hemoglobin Ty GARD (alphaA2beta2 124 (H2) Pro replaced by Gln). A stable high O2 affinity variant at the alpha1beta1 contact. FEBS Lett. 1978;88(1):155–159.
- Wajcman H, Kister J, Prehu C, et al. Hb Tende [β124(H2)Pro→Leu]: a new variant with a moderate increase in oxygen affinity. Hemoglobin 1998;22(5-6):517–523.
- Clegg JB, Weatherall DJ, Boon WH, et al. Two new haemoglobin variants involving proline substitutions. Nature 1969;222(5191):379–380.
- P Warghade S C, Chanekar M, et al. A rare hemoglobin variant: Hb Ty Gard detected in an Indian family. Indian J Pathol Oncol 2014;1(1):37–40.
- Hendy JG, Garofalo K, Bowden DK. Hb Khartoum [β124(H2)Pro→Arg] in a Vietnamese female. Hemoglobin 1999;23(3):291–293.
- Sangkitporn SK, Eksiri L, Sangnoi A, et al. Identification of beta-globin gene mutations in Thailand using an automated fluorescence-based DNA sequencer. Int J Lab Hematol. 2009;31(5):521–527.
- Benson JM, Therrell BL. Jr., History and current status of newborn screening for hemoglobinopathies. Semin Perinatol. 2010;34(2):134–144.