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Hemoglobin
international journal for hemoglobin research
Volume 27, 2003 - Issue 2
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Original

A new Unstable α2‐Globin Gene Variant: Hb Chartres [α33(B14)Phe→Ser]

Claude Préhu Génétique Moléculaire et Physiopathologie, INSERM U468 and Service de Biochimie, Hôpital Henri Mondor AP‐HP, 51 Avenue du Marechal de Lattre de Tassigny, Créteil, 94010, France
,
Elodie Mazurier Génétique Moléculaire et Physiopathologie, INSERM U468 and Service de Biochimie, Hôpital Henri Mondor AP‐HP, 51 Avenue du Marechal de Lattre de Tassigny, Créteil, 94010, France
,
Jean Riou Génétique Moléculaire et Physiopathologie, INSERM U468 and Service de Biochimie, Hôpital Henri Mondor AP‐HP, 51 Avenue du Marechal de Lattre de Tassigny, Créteil, 94010, France
,
Jean Kister INSERM U473, Le Kremlin Bicêtre Cedex, France
,
Danielle Promé Institut de Chimie Moléculaire Paul Sabatier1744, Toulouse, France
,
Suzy Richelme‐David Institut de Chimie Moléculaire Paul Sabatier1744, Toulouse, France
,
Lina Al Jassem Hôpitaux de Chartres, Onco‐hématologie, Chartres Cedex, France
,
Elisabeth Angellier Hôpitaux de Chartres, Onco‐hématologie, Chartres Cedex, France
&
Dr. Henri Wajcman Génétique Moléculaire et Physiopathologie, INSERM U468 and Service de Biochimie, Hôpital Henri Mondor AP‐HP, 51 Avenue du Marechal de Lattre de Tassigny, Créteil, 94010, France
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Pages 111-115 | Received 13 Sep 2002, Accepted 20 Nov 2002, Published online: 07 Jul 2009

Citations (8)

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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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Joanne Traeger-Synodinos, Varvara Douna, Ioannis Papassotiriou, Alexandra Stamoulakatou, Vasilis Ladis, Tania Siahanidou, Irine Fylaktou & Emmanuel Kanavakis. (2010) Variable and Often Severe Phenotypic Expression in Patients with the α-Thalassemic Variant Hb Agrinio [α29(B10)Leu→Pro (α2)]. Hemoglobin 34:5, pages 430-438.
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Varvara Douna, Ioannis Papassotiriou, Anna Metaxotou-Mavrommati, Alexandra Stamoulakatou, Dimitra Liapi, Dimitrios Kampourakis, Amalia Tsilimigaki, Emmanuel Kanavakis & Joanne Traeger-Synodinos. (2008) Further Identification of The Hyperunstable α-Globin Chain Variant Hb Heraklion [codons 36/37 (–CCC); Pro→0 (α1)] in Greek Cases With Co-Inherited α+-Thalassemia Mutations. Hemoglobin 32:4, pages 379-385.
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Varvara Douna, Ioannis Papassotiriou, Anastasia Garoufi, Eleni Georgouli, Vassilis Ladis, Alexandra Stamoulakatou, Anna Metaxotou-Mavrommati, Emmanuel Kanavakis & Joanne Traeger-Synodinos. (2008) A Rare Thalassemic Syndrome Caused by Interaction of Hb Adana [α59(E8)Gly→Asp] with an α+-Thalassemia Deletion: Clinical Aspects in Two Cases. Hemoglobin 32:4, pages 361-369.
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Henri Wajcman, Jan Traeger-Synodinos, Ioannis Papassotiriou, Piero C. Giordano, Cornelis L. Harteveld, Véronique Baudin-Creuza & John Old. (2008) Unstable and Thalassemic α Chain Hemoglobin Variants: A Cause of Hb H Disease and Thalassemia Intermedia. Hemoglobin 32:4, pages 327-349.
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Cornelis L. Harteveld, Mark Vervloet, Sonja Zweegman, Peter van Delft, Nicole Akkermans, Sandra Arkestijn & Piero C. Giordano. (2005) Hb Amsterdam [α32(B13)Met→Ile (α2)]: A New Unstable Variant Associated with an α-Thalassemia Phenotype and a New African Polymorphism. Hemoglobin 29:4, pages 257-262.
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Articles from other publishers (2)

Martin H. Steinberg, Bernard G. Forget, Douglas R. Higgs & David J. Weatherall. 2010. Disorders of Hemoglobin. Disorders of Hemoglobin 241 265 .
Martin H. Steinberg, Bernard G. Forget, Douglas R. Higgs & David J. WeatherallDouglas R. Higgs. 2010. Disorders of Hemoglobin. Disorders of Hemoglobin 239 240 .

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