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Hemoglobin
international journal for hemoglobin research
Volume 18, 1994 - Issue 6
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Original Article

β-Thalassemia intermedia in a lebanese child due to homozygosity for the -88 (C→T) Mutation

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Pages 383-388 | Received 15 Jul 1994, Accepted 20 Oct 1994, Published online: 07 Jul 2009

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Othman E. Soliman, Sohier Yahia, Amany Shouma, Hala K. Shafiek, Ashraf E. Fouda, Hanan Azzam, Nashwa K. Abousamra, Rabab Mahfouz, Enas F. Goda & Solafa A. El-Sharawy. (2010) Reverse hybridization StripAssay detection of β-thalassemia mutations in northeast Egypt. Hematology 15:3, pages 182-186.
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Mohammad T. Akbari, Pantea Izadi, Mina Izadyar, Kyriacou Kyriacou & Marina Kleanthous. (2008) Molecular Basis of Thalassemia Intermedia in Iran. Hemoglobin 32:5, pages 462-470.
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Articles from other publishers (3)

N. J. Makhoul, R. S. Wells, H. Kaspar, H. Shbaklo, A. Taher, N. Chakar & P. A. Zalloua. (2005) Genetic Heterogeneity of Beta Thalassemia in Lebanon Reflects Historic and Recent Population Migration. Annals of Human Genetics 69:1, pages 55-66.
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A. NADKARNI, T. SAKAGUCHI, A. GORAKSHAKAR, S. PHANASGAONKAR, R. KIYAMA, R. COLAH & D. MOHANTY. (2004) An interplay of alleviating mutations in the clinical phenotype of beta-thalassaemia intermedia. Clinical and Laboratory Haematology 26:6, pages 419-422.
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G.O. Tadmouri, Ş. Tüzmen, H. Özçelik, A. Özer, S.M. Baig, E.B. Senga & A.N. Başak. (1998) Molecular and population genetic analyses of β-Thalassemia in Turkey. American Journal of Hematology 57:3, pages 215-220.
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