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Hemoglobin
international journal for hemoglobin research
Volume 10, 1986 - Issue 4
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Original Article

The Effect of α-Thalassemia on the Level of Hybrid Hemoglobin Variants in Heterozygotes

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Pages 401-416 | Received 08 Jan 1986, Accepted 13 Mar 1986, Published online: 07 Jul 2009

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C. Öner, R. Öner, H. Balkan, F. Gümrük & A. Gürgey. (1998) Coexistence of Hb Lepore-Boston-Washington (δ87GLN-β-IVS-II-8) With α-Thalassemia [α(-5NT)α/αα]. Hemoglobin 22:3, pages 273-276.
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C. Altay, A. Kutlar, J. B. Wilson, B. B. Webber & T. H.J. Huisman. (1987) HB P-Nilotic or α2(βδ)2 in a Turkish Family. Hemoglobin 11:4, pages 395-399.
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Articles from other publishers (2)

John S. Waye, David H. K. Chui, Shi‐Ping Cai, Barry Eng & William H. Francombe. (2006) Clinical course and molecular characterization of a compound heterozygote for sickle hemoglobin and hemoglobin kenya. American Journal of Hematology 41:4, pages 289-291.
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Jing-Zhong Liu, Teruo Harano, Kenneth D. Lanclos & Titus H.J. Huisman. (1987) The β-δ crossover leading to the βδ hybrid gene of hemoglobin P-Nilotic is located within 54 base-pairs of the 5′ end of exon 2 or between codons 31 and 50. Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression 909:3, pages 208-212.
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