Molecular spectrum of α-thalassemia mutations in Erbil province of Iraqi Kurdistan

Galanello R, Cao A (2011) Alpha-thalassemia. Genet Med 13:83–88

Valaei A, Karimipoor M, Kordafshari A et al (2018) Molecular basis of α-thalassemia in Iran. Iran Biomed J 22:6

Borgio JF (2015) Molecular nature of alpha-globin genes in the Saudi population. Saudi Med J 36:1271

Piel FB, Weatherall DJ (2014) The α-thalassemias. N Engl J Med 371:1908–1916

Panigrahi I, Marwaha R (2007) Mutational spectrum of thalassemias in India. Indian J Hum Genet 13:36

Birgens H, Ljung R (2007) The thalassaemia syndromes. Scand J Clin Lab Invest 67:11–26

Akhtar MS, Qaw F, Borgio JF et al (2013) Spectrum of α-thalassemia mutations in transfusion-dependent β-thalassemia patients from the Eastern Province of Saudi Arabia. Hemoglobin 37:65–73

Farashi S, Harteveld CL (2018) Molecular basis of α-thalassemia. Blood Cells Mol Dis 70:43–53

Dh CHUI (2005) α-Thalassemia: Hb H disease and Hb Barts hydrops fetalis. Ann N Y Acad Sci 1054:25–32

Flint J, Harding RM, Boyce AJ et al (1998) The population genetics of the haemoglobinopathies. Baillieres Clin Haematol 11:1–51

Polus RK (2017) Prevalence of hemoglobinopathies among marrying couples in Erbil province of Iraq. Iraqi J Hemat 6:90–93

Al-Allawi NA, Hassan K, Sheikha AK et al (2010) β-Thalassemia mutations among transfusion-dependent Thalassemia major patients in Northern Iraq. Mol Biol Int 2010:479282

Shamoon RP, Al-Allawi NA, Cappellini MD et al (2015) Molecular basis of β-thalassemia intermedia in Erbil province of Iraqi Kurdistan. Hemoglobin 39:178–183

Al-Allawi NA, Badi AI, Imanian H et al (2009) Molecular characterization of α-thalassemia in the Dohuk region of Iraq. Hemoglobin 33:37–44

Al-Allawi NA, Jalal SD, Rasheed NS et al (2013) The spectrum of α-thalassemia mutations in the Kurdish population of Northeastern Iraq. Hemoglobin 37:56–64

Dehbozorgian J, Moghadam M, Daryanoush S et al (2015) Distribution of alpha-thalassemia mutations in Iranian population. Hematology 20:359–362

Bozdogan ST, Yuregir OO, Buyukkurt N et al (2015) Alpha-thalassemia mutations in Adana Province, southern Turkey: genotype–phenotype correlation. Indian J Hematol Blood Transfus 31:223–228

Celik MM, Gunesacar R, Oktay G et al (2013) Spectrum of α-thalassemia mutations including first observation of-FIL deletion in Hatay Province. Turkey Blood Cells Mol Dis 51:27–30

Hadavi V, Taromchi AH, Malekpour M et al (2007) Elucidating the spectrum of α-thalassemia mutations in Iran. Haematologica 92:992–993

Kamal N, Shbailat T (2008) Molecular spectrum of alpha-thalassemia in Jordan. JRMS 15:23–27

Baysal E (2011) α-Thalassemia syndromes in the United Arab Emirates. Hemoglobin 35:574–580

Jassim N, Al-Arrayed S, Gerard N et al (2001) Molecular basis of α-thalassemia in Bahrain. Bahrain Med Bull 23:3–7

Baysal E, Kleanthous M, Bozkurt G et al (1995) α-Thalassaemia in the population of Cyprus. Br J Haematol 89:496–499

Kanavakis E, Papassotiriou I, Karagiorga M et al (2000) Phenotypic and molecular diversity of haemoglobin H disease: a Greek experience. Br J Haematol 111:915–923

Hellani A, Fadel E, El-Sadadi S et al (2009) Molecular spectrum of α-thalassemia mutations in microcytic hypochromic anaemia patients from Saudi Arabia. Genet Test Mol Biomarkers 13:219–221

Laosombat V, Viprakasit V, Chotsampancharoen T et al (2009) Clinical features and molecular analysis in Thai patients with HbH disease. Ann Hematol 88:1185–1192

Whitelaw E (1986) Proudfoot N (1986) Alpha-thalassaemia caused by a poly(A) site mutation reveals that transcriptional termination is linked to 3′ end processing in the human alpha 2 globin gene. EMBO J 5:2915–2922