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Hemoglobin
international journal for hemoglobin research
Volume 25, 2001 - Issue 1
56
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Original

Hb SITIA [β128(H6)Ala→Val]: AN UNSTABLE VARIANT WITH A SUBSTITUTION IN THE α1β1 INTERFACE

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Pages 45-56 | Received 13 Jun 2000, Accepted 08 Sep 2000, Published online: 07 Jul 2009

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Ioannis Papassotiriou, Alexandra Stamoulakatou, Henri Wajcman, Jean Kister, Gerasimos Dimisianos, Christina Lazaropoulou, Ino Kanavaki, Efstathios Vavourakis, Antonios Kattamis, Emmanuel Kanavakis & Joanne Traeger-Synodinos. (2006) Observation of a Rare Hemoglobin Variant [Hb Lulu Island, β107(G9)Gly→Asp, GGC→GAC] Co-Inherited With a β+-Thalassemia Mutation [IVS-I-110 (G→A)] or in the Heterozygous State in a Greek-Albanian Family. Hemoglobin 30:4, pages 409-418.
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Henri Wajcman, Agnés Lahary, Danielle Promé, Jean Kister, Jean Riou, Christian Godart, Claude Préhu, Jan Traeger-Synodinos, Ioannis Papassotiriou & Frederic Galactéros. (2001) Hb MONT SAINT AIGNAN [β128(H6)Ala → Pro]: A NEW UNSTABLE VARIANT LEADING TO CHRONIC MICROCYTIC ANEMIA. Hemoglobin 25:1, pages 57-65.
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Articles from other publishers (1)

Ioannis Papassotiriou, Joanne Traeger-Synodinos, Michael C. Marden, Jean Kister, Dimitra Liapi, Danielle Prome, Alexandra Stamoulakatou, Henri Wajcman & Emmanuel Kanavakis. (2005) The homozygous state for Hb Crete [β129 (H7) Ala→Pro] is associated with a complex phenotype including erythrocytosis and functional anemia. Blood Cells, Molecules, and Diseases 34:3, pages 229-234.
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