References
- Bernini L F. Geographic distribution of α thalassemia. In: Steinberg M H, Forget B G, Higgs D R, Nagel R L, eds. Disorders of Hemoglobin: Genetics, Pathophysiology, and Clinical Management. Cambridge: Cambridge University Press, 2001:878–894.
- Higgs D R, Vickers M A, Wilkie A OM, Pretorius I-M, Jarman A P, Weatherall D J. A review of the molecular genetics of the human α-globin gene cluster. Blood 1989; 73(5):1081–1104. [PUBMED], [INFOTRIEVE]
- Higgs D R, Bowden D K. Clinical and laboratory features of the α-thalassemia syndromes. In: Steinberg M H, Forget B G, Higgs D R, Nagel R L, eds. Disorders of Hemoglobin: Genetics, Pathophysiology, and Clinical Management. Cambridge, Cambridge University Press, 2001:431–469.
- Kazazian H H Jr. The thalassemia syndromes: molecular basis and prenatal diagnosis. Semin Hematol 1990; 27(3):209–228. [PUBMED], [INFOTRIEVE]
- Chong S S, Boehm C D, Higgs D R, Cutting G R. Single tube multiplex-PCR screen for common deletional determinants of α-thalassemia. Blood 2000; 95(1):360–362. [PUBMED], [INFOTRIEVE], [CSA]
- Chui D HK, Fucharoen S, Chan V. Hemoglobin H disease: not necessarily a benign disorder. Blood 2003; 101(3):791–800. [PUBMED], [INFOTRIEVE], [CSA], [CROSSREF]
- Liu Y T, Old J M, Miles K, Fisher C A, Weatherall D J, Clegg J B. Rapid detection of α-thalassaemia deletions and α-globin gene triplication by multiplex polymerase chain reactions. Br J Haematol 2000; 108(2):295–299. [PUBMED], [INFOTRIEVE], [CSA], [CROSSREF]
- Tan A S, Quah T C, Low P S, Chong S S. A rapid and reliable 7-deletion multiplex polymerase chain reaction assay for α-thalassemia. Blood 2001; 98(1):250–251. [PUBMED], [INFOTRIEVE], [CSA], [CROSSREF]
- Anderson H M, Ranney H M. Southeast Asian immigrants: the new thalassemias in Americans. Semin Hematol 1990; 27(3):239–246. [PUBMED], [INFOTRIEVE]
- Chui D HK, Waye J S. Hydrops fetalis caused by α-thalassemia: an emerging health care problem. Blood 1998; 91(7):2213–2222., [PUBMED], [INFOTRIEVE], [CSA]
- Available from the 2001 Canadian census at: www.statcan.ca. Accessed May 2004.
- Available from Global Consensus Standardization for Health Technologies at www.nccls.org. Accessed May 2004.
- Mentzer W C Jr. Differentiation of iron deficiency from thalassaemia trait. Lancet 1973; i(7808):882, [CROSSREF]
- Borges E, Wenning M RSC, Kimura E M, Gervàsio S A, Costa F F, Sonati M F. High prevalence of α-thalassemia among indviduals with microcytosis and hypochromia without anemia. Braz J Med Biol Res 2001; 34(6):759–762. [PUBMED], [INFOTRIEVE], [CSA]
- Sivera P, Roetto A, Mazza U, Camaschella C. Feasibility of molecular diagnosis of α-thalassemia in the evaluation of microcytosis. Haematologica 1997; 82(5):592–593. [PUBMED], [INFOTRIEVE], [CSA]
- Rees D C, Williams T N, Maintland K, Clegg J B, Weatherall D J. α Thalassaemia is associated with increased soluble transferrin receptor levels. Br J Haematol 1998; 103(2):368–369. [CROSSREF]