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Hemoglobin
international journal for hemoglobin research
Volume 25, 2001 - Issue 1
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Hb MONT SAINT AIGNAN [β128(H6)Ala → Pro]: A NEW UNSTABLE VARIANT LEADING TO CHRONIC MICROCYTIC ANEMIA

Henri Wajcman INSERM U 468 and Department of Biochemistry, Hôpital Henri Mondor, Créteil, AP-HP 94010, France; INSERM U468, Department of Biochemistry, Hôpital Henri Mondor, 51 Avenue du Marechal de Lattre de Tassigny, Créteil, AP-HP 94010, France
,
Agnés Lahary
,
Danielle Promé Institut de Chimie Moléculaire Paul Sabatier, FR 1744, Toulouse, Cedex 4, 31062, France
,
Jean Kister
,
Jean Riou INSERM U 468 and Department of Biochemistry, Hôpital Henri Mondor, Créteil, AP-HP 94010, France
,
Christian Godart INSERM U 468 and Department of Biochemistry, Hôpital Henri Mondor, Créteil, AP-HP 94010, France
,
Claude Préhu INSERM U 468 and Department of Biochemistry, Hôpital Henri Mondor, Créteil, AP-HP 94010, France
,
Jan Traeger-Synodinos First Department of Pediatrics, Athens University, “Aghia Sophia” Children’s Hospital, Athens, 11 527, Greece
,
Ioannis Papassotiriou Laboratory of Clinical Chemistry, “Aghia Sophia” Children’s Hospital, Athens, 11 527, Greece
&
Frederic Galactéros INSERM U 468 and Department of Biochemistry, Hôpital Henri Mondor, Créteil, AP-HP 94010, France
 show all
Pages 57-65 | Received 16 Jun 2000, Accepted 10 Aug 2000, Published online: 07 Jul 2009

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Yan Li, Jin-Mei Yan, Jian-Ying Zhou, Yue-Cheng Lu & Dong-Zhi Li. (2017) Combination of Hb Heze [β144(HC1)Lys→Arg; HBB: c.434A>G] and β0-Thalassemia in a Chinese Patient with β-Thalassemia Intermedia. Hemoglobin 41:1, pages 47-49.
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Georgia Christopoulou, Aggeliki Tserga, George P. Patrinos & Manoussos N. Papadakis. (2004) Molecular Characterization and Diagnosis of Hb Crete [β129(H7)Ala→Pro]. Hemoglobin 28:4, pages 339-342.
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Ioannis Papassotiriou, Joanne Traeger-Synodinos, Danielle Promé, Jean Kister, Christina Vrettou, Athina Xaidara, Michael Marden, Alexandra Stamoulakatou, Henri Wajcman & Emmanuel Kanavakis. (2001) Hb SITIA [β128(H6)Ala→Val]: AN UNSTABLE VARIANT WITH A SUBSTITUTION IN THE α1β1 INTERFACE. Hemoglobin 25:1, pages 45-56.
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Articles from other publishers (4)

Isabelle Zanella-Cleon, Philippe Joly, Michel Becchi & Alain Francina. (2009) Phenotype determination of hemoglobinopathies by mass spectrometry. Clinical Biochemistry 42:18, pages 1807-1817.
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Martin H. Steinberg, Bernard G. Forget, Douglas R. Higgs & David J. WeatherallSwee Lay Thein & William G. Wood. 2010. Disorders of Hemoglobin. Disorders of Hemoglobin 323 356 .
Martin H. Steinberg, Bernard G. Forget, Douglas R. Higgs & David J. Weatherall. 2010. Disorders of Hemoglobin. Disorders of Hemoglobin 321 322 .
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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