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Hemoglobin
international journal for hemoglobin research
Volume 34, 2010 - Issue 6
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A Dyserythropoietic Anemia Associated with Homozygous Hb Plasencia [α125(H8)Leu→Arg (α2)] (HBA2:c.377T>G), A Variant with an Unstable α Chain

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Pages 576-581 | Received 28 Jul 2010, Accepted 06 Sep 2010, Published online: 15 Nov 2010

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Elizabete Cunha, Celeste Bento, Ana Oliveira, Luís Relvas, Joana Neves, Mariline Gameiro, Cristina Barros, Ana Araújo, Ana Macedo, Paula Rocha, Ricardo Costa, Tabita Maia & M. Letícia Ribeiro. (2013) Hb Plasencia [α125(H8)Leu→Arg (α2)] is a Frequent Cause of α+-Thalassemia in the Portuguese Population. Hemoglobin 37:2, pages 183-187.
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Celeste Bento, Ana Catarina Oliveira, Joana Neves, Mariline Gameiro, Elizabete Cunha, Margarida Coucelo, Ricardo Marques Costa, José Barbot, Emilia Costa, Carlos Fernández-Lago & M. Leticia Ribeiro. (2012) Hb Iberia [α104(G11)Cys → Arg,TGC>CGC (α2) (HBA2:c.313T>C)], a New α-Thalassemic Hemoglobin Variant Found in the Iberian Peninsula: Report of Six Cases. Hemoglobin 36:6, pages 517-525.
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Articles from other publishers (1)

Barbara J. Bain, David M. Clark & Bridget S. Wilkins. 2019. Bone Marrow Pathology. Bone Marrow Pathology 585 644 .

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