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Hemoglobin
international journal for hemoglobin research
Volume 36, 2012 - Issue 2
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Short Communications

A Rare Hb H Disease Due to the – –SEA and 16.6 kb α-Thalassemia-2 Deletions

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Pages 200-204 | Received 11 Sep 2011, Accepted 27 Nov 2011, Published online: 29 Feb 2012

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Wittaya Jomoui, Wanicha Tepakhan, Surada Satthakarn & Sitthichai Panyasai. (2020) Molecular spectrum of Hb H disease and characterization of rare deletional α-thalassemia found in Thailand. Scandinavian Journal of Clinical and Laboratory Investigation 80:7, pages 528-535.
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Articles from other publishers (3)

Walaiporn Yimniam & Sumalee Jindadamrongwech. (2016) Scanning for α-Hemoglobin Variants by High-Resolution Melting Analysis. Journal of Clinical Laboratory Analysis 30:5, pages 633-640.
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Attawut Chaibunruang, Rossarin Karnpean, Goonnapa Fucharoen & Supan Fucharoen. (2014) Genetic heterogeneity of hemoglobin AEBart's disease: A large cohort data from a single referral center in northeast Thailand. Blood Cells, Molecules, and Diseases 52:4, pages 176-180.
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Luxin Yu, Wei Wu, Puchang Lie, Yunhua Liu & Lingwen Zeng. (2013) Isothermal Strand-Displacement Polymerase Reaction for Visual Detection of the Southeast Asian–Type Deletion of α-Thalassemia. The Journal of Molecular Diagnostics 15:6, pages 776-782.
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