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Hemoglobin
international journal for hemoglobin research
Volume 39, 2015 - Issue 3
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Original Article

Hb Dartmouth (HBA2: c.200T>C): An α2-Globin Gene Associated with Hb H Disease in One Homozygous Patient

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Pages 152-155 | Received 11 Sep 2014, Accepted 12 Dec 2014, Published online: 15 May 2015

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Read on this site (3)

Agathe Horri-Naceur & David J. Timson. (2020) In Silico Analysis of the Effects of Point Mutations on α-Globin: Implications for α-Thalassemia. Hemoglobin 44:2, pages 89-103.
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Samaneh Farashi, Negin F. Garous, Shadi Vakili, Mehri Ashki, Hashem Imanian, Azita Azarkeivan & Hossein Najmabadi. (2016) Characterization of Homozygous Hb Setif (HBA2: c.283G>T) in the Iranian Population. Hemoglobin 40:1, pages 53-55.
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Samaneh Farashi, Nooshin Bayat, Shadi Vakili, Negin Faramarzi Garous, Mehri Ashki, Hashem Imanian, Hossein Najmabadi & Azita Azarkeivan. (2016) Point mutations which should not be overlooked in Hb H disease. Expert Review of Hematology 9:1, pages 107-113.
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Articles from other publishers (2)

Barbara J. Bain. 2020. Haemoglobinopathy Diagnosis. Haemoglobinopathy Diagnosis 85 184 .
Samaneh Farashi & Hossein Najmabadi. (2015) Diagnostic pitfalls of less well recognized HbH disease. Blood Cells, Molecules, and Diseases 55:4, pages 387-395.
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