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Hemoglobin
international journal for hemoglobin research
Volume 14, 1990 - Issue 5
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Original Article

B Sun Prae or α2130(H13)Au → Pr0β2 Second Observation In An Indian Adult

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Pages 491-497 | Published online: 07 Jul 2009

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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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Prashant Deshpande, Neelagandan Kamalanathan, Eswari Sampath, Biju George, Ramachandran V. Shaji & Eunice S. Edison. (2015) Characterization of Clinical and Laboratory Profiles of the Deletional α2-Globin Gene Polyadenylation Signal Sequence (AATAAA > AATA– –) in an Indian Population. Hemoglobin 39:6, pages 415-418.
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Ahmad Tamaddoni, Valeh Hadavi, Nima Hafezi Nejad, Atefeh Khosh-Ain, Rita Siami, Jalil Aghai-Meibodi, Navid Almadani, Christian Oberkanins, Hai-Yang Law & Hossein Najmabadi. (2009) α-Thalassemia Mutation Analyses in Mazandaran Province, North Iran. Hemoglobin 33:2, pages 115-123.
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M. F. H. Carver & T. H. J. Huisman. (1997) International Hemoglobin Information Center Variant List. Hemoglobin 21:6, pages 505-506.
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. (1996) Variants of the Alpha Chain. Hemoglobin 20:3, pages 215-312.
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P. J. Ho, J. Rochette, D. C. Rees, C. A. Fisher, E. R. Huehns, A. M. Will & S. L. Thein. (1996) Hb Sun Prairie: Diagnostic Pitfalls in Thalassemic Hemoglobinopathies. Hemoglobin 20:2, pages 103-112.
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. (1994) International Hemoglobin Information Center. Hemoglobin 18:2, pages 77-161.
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. (1993) Variants of the Alpea Chain. Hemoglobin 17:2, pages 89-177.
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. (1992) Variants of the Alpha Chain. Hemoglobin 16:3, pages 127-213.
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Articles from other publishers (4)

Ankur Jain, Pooja Prasad, Sumita Chaudhry, D.K. Gupta & Sumita Saluja. (2021) Hb Sun Prairie: A rare cause of chronic hemolysis in an Indian patient. Hematology/Oncology and Stem Cell Therapy 14:3, pages 257-259.
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Paloma Ropero, Jorge M. Nieto, Fernando-Ataúlfo González Fernández, Ana Villegas & Celina Benavente. (2021) Hb Maruchi [α165 (E14) Ala>Pro; HBA1: c.196G>C]: A new thalassemia hemoglobinopathy related to the alpha1 globin gene. Clinical Biochemistry 92, pages 77-81.
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S. Nair, A. Nadkarni, P. Warang, A. Bhave, K. Ghosh & R. Colah. (2010) Five α globin chain variants identified during screening for haemoglobinopathies. European Journal of Clinical Investigation 40:3, pages 226-232.
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H. Wajcman, C. Vasseur, Y. Blouquit, J. Rosa, D. Labie, A. Najman, O. Reman, M. Leporrier & F. Galacteros. (1993) Unstable alpha-chain hemoglobin variants with factitious beta-thalassemia biosynthetic ratio: Hb questembert (α131[H14] Ser→Pro) and Hb Caen (α132[H15] Val→Gly). American Journal of Hematology 42:4, pages 367-374.
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