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Hemoglobin
international journal for hemoglobin research
Volume 7, 1983 - Issue 3
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Original Article

Hemoglobin Leiden [β6 or 7 (A3 or A4) GLU → 0] in a Yugoslavian Woman Arisen by a New Mutation

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Pages 271-277 | Received 02 Dec 1982, Accepted 24 Feb 1983, Published online: 07 Jul 2009

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Marco Rosetti, Giovanni Poletti, Alberto Sensi, Anna Ravani, Michela Rondoni, Luca Baldrati & Romolo M. Dorizzi. (2015) A rare case of Hemoglobin Leiden interfering with the DIFF channel of Sysmex XE-2100. Scandinavian Journal of Clinical and Laboratory Investigation 75:5, pages 436-437.
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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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J. D. Hoyer, M. J. Wick, K. Snow, W. Finkelstein & V. F. Fairbanks. (1999) DNA Sequence Analysis of Hb Leiden [β6(A3) or β7(A4) Ghi→0]. Hemoglobin 23:3, pages 299-301.
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J. B. Wilson, S. S. Chen, B. B. Webber, A. Kutlar, F. Kutlar, A. Villegas & T. H. J. Huisman. (1986) The Identification of Five Rare β-Chain Abnormal Hemoglobins by High Performance Liquid Chromatographic Procedures. Hemoglobin 10:1, pages 49-63.
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Articles from other publishers (1)

Juan R. Alvarez-Dominguez, Olga Amosova & Jacques R. Fresco. (2013) Self-catalytic DNA Depurination Underlies Human β-Globin Gene Mutations at Codon 6 That Cause Anemias and Thalassemias. Journal of Biological Chemistry 288:16, pages 11581-11589.
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