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Hemoglobin
international journal for hemoglobin research
Volume 28, 2004 - Issue 2
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Short Communication

A Rare 33 bp In‐Frame Deletion (α63–74 or α64–74 or α65–75) in the α1‐Globin Gene Causing α+‐Thalassemia: A Second Observation

Gerasimos Dimisianos Medical Genetics, Athens University, “Aghia Sophia” Children's Hospital, Thivon and Levadias Streets, Athens, 11527, Greece
, D.Phil. (Oxon),
Joanne Traeger‐Synodinos Medical Genetics, Athens University, “Aghia Sophia” Children's Hospital, Thivon and Levadias Streets, Athens, 11527, Greece
, D.Phil. (Oxon),
Christina Vrettou Medical Genetics, Athens University, “Aghia Sophia” Children's Hospital, Thivon and Levadias Streets, Athens, 11527, Greece
, D.Phil. (Oxon),
Ioannis Papassotiriou Department of Clinical Biochemistry, “Aghia Sophia” Children's Hospital, Athens, Greece
, D.Phil. (Oxon) &
Emmanuel Kanavakis Medical Genetics, Athens University, “Aghia Sophia” Children's Hospital, Thivon and Levadias Streets, Athens, 11527, Greece
, D.Phil. (Oxon)
Pages 137-143 | Received 13 Nov 2004, Accepted 29 Dec 2004, Published online: 24 Aug 2009

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Yin-Sheng Zhai, Hai-Shen Tang, Jian-Ying Zhou & Dong-Zhi Li. (2012) A Novel Case of Hb Phnom Penh: Codons 117/118 (+ATC) as a Cause of α+-Thalassemia. Hemoglobin 36:3, pages 289-292.
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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, Alexandra Stamoulakatou, Anna Metaxotou-Mavrommati, Emmanuel Kanavakis & Joanne Traeger-Synodinos. (2008) Association of Mild and Severely Unstable α Chain Variants: The First Observation of a Compound Heterozygote with Hb Setif [α94(G1)Asp→Tyr (α2)] and Hb Agrinio [α29(B10)Leu→Pro (α2)] in a Greek Family. Hemoglobin 32:6, pages 592-595.
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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, Dimitra Liapi, Dimitrios Kampourakis, Zoe Repapinou, Ioannis Papassotiriou, Alexandra Stamoulakatou, Christos Poziopoulos, Emmanuel Kanavakis & Joanne Traeger-Synodinos. (2008) First Observation of Hb Taybe [Codons 38/39 (−Acc) Thr→0 (α1)] In Greece: Clinical and Hematological Findings in Patients With Co-Inherited α+-Thalassemia Mutations. Hemoglobin 32:4, pages 371-378.
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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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