REFERENCES
- Muncie H, Campbell JS. Alpha and beta thalassemia. Am Fam Physician. 2009;80:339–344.
- Chui DH, Fucharoen S, Chan V. Hemoglobin H disease: not necessarily a benign disorder. Blood. 2003;101:791–800.
- Kılınç Y, Gürgey A, Kümi M, Altay Ç. Adana bölgesinde doğan bebeklerde kordon kanı çalışması ile alfa talasemi, G6PD enzim eksikliği ve HbS sıklığının araştırılması. Doğa. 1986;10:162–167.
- Ferrara M, Coppola L, Coppola A, Iron deficiency in childhood and adolescence: retrospective review. Hematology. 2006;11:183–186.
- Tadmouri GO, Tüzmen S, Ozcelik H, Molecular and population genetic analyses of β-thalassemia in Turkey. Am J Hematol. 1998;57:215–220.
- Irken G, Oren H, Undar B, Analysis of thalassemia syndromes and abnormal hemoglobins in patients from the Aegean region of Turkey. Turk J Pediatr. 2002;44:21–24.
- Kanavakis E, Papassotirou I, Karagiorga M, Phenotypic and molecular diversity of haemoglobin H disease: a Greek experience. Br J Haematol. 2000;111:915–923.
- Baysal E, Kleanthous M, Bozkurt G, α-Thalassaemia in the population of Cyprus. Br J Haematol. 1995;89:496–499.
- Fattoum S, Abbes S, Ben Abdeladhim A, Detection of alpha-thalassemia in Tunisia (across 1500 cases). Tunis Med. 1987 Dec;65(12):763–766.
- Zorai A, Abbes S, Prehu C, Hb H disease among Tunisians: molecular characterization of alpha-thalassemia determinants and hematological findings. Hemoglobin. 2003;27:57–61.
- Siala H, Ouali F, Messaoud T, alpha-Thalassaemia in Tunisia: some epidemiological and molecular data. J Genet. 2008;87:229–234.
- Sorour Y, Heppinstall S, Porter N, Is routine molecular screening for common alpha-thalassaemia deletions necessary as part of an antenatal screening programme? J Med Screen. 2007;14:60–61.
- Panomai N, Sanchaisuriya K, Yamsri S, Thalassemia and iron deficiency in a group of northeast Thai school children: relationship to the occurrence of anemia. Eur J Pediatr. 2010;169:1317–1322.
- Di Bella C, Salpietro C, La Rosa M, Identification of alpha-thalassemia mutations in subjects from Eastern Sicily (Italy) with abnormal hematological indices and normal Hb A2. Ann Hematol. 2006;85:829–831.
- Oner C, Gürgey A, Oner R, The molecular basis of Hb H disease in Turkey. Hemoglobin. 1997;21:41–51.
- Guvenc B, Yildiz SM, Tekinturhan F, Molecular characterization of alpha-Thalassemia in Adana, Turkey: a single center study. Acta Haematol. 2010;123:197–200.