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Adams, Robert J (2013) Toward a stroke-free childhood in sickle cell disease: the 2013 Sherman Lecture. Stroke 44:2930-4
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Schiliro, G; Di Gregorio, F; Samperi, P et al. (1995) Genetic heterogeneity of beta-thalassemia in southeast Sicily. Am J Hematol 48:5-11
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Baysal, E; Huisman, T H (1994) Detection of common deletional alpha-thalassemia-2 determinants by PCR. Am J Hematol 46:208-13
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Efremov, D G; Dimovski, A J; Baysal, E et al. (1994) Possible factors influencing the haemoglobin and fetal haemoglobin levels in patients with beta-thalassaemia due to a homozygosity for the IVS-I-6 (T-->C) mutation. Br J Haematol 86:824-30
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Goncalves, M S; Sonati, M F; Kimura, M et al. (1994) Association of Hb Santa Ana [alpha 2 beta (2)88(F4)Leu- > Pro] and Hb Porto Alegre [alpha 2 beta (2)9(A6)Ser- > Cys] in a Brazilian female. Hemoglobin 18:235-9
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Baysal, E; Ribeiro, M L; Huisman, T H (1994) Binding of nuclear factors to the proximal and distal CACCC motifs of the beta-globin gene promoter: implications for the -101 (C-->T) 'silent' beta-thalassemia mutation. Acta Haematol 91:16-20
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Divoky, V; Baysal, E; Oner, R et al. (1994) The T-->C mutation at position +96 of the untranslated region 3' to the terminating codon of the beta-globin gene is a rare polymorphism that does not cause a beta-thalassemia as previously ascribed. Hum Genet 93:77-8
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