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Hemoglobin
international journal for hemoglobin research
Volume 32, 2008 - Issue 4
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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

Varvara Douna Hematology Laboratory, “P. and A. Kyriakou” Children's Hospital, Athens, Greece
,
Ioannis Papassotiriou Department of Clinical Biochemistry, “Aghia Sophia” Children's Hospital, Athens, Greece
,
Anna Metaxotou-Mavrommati Department of Medical Genetics, University of Athens, “Aghia Sophia” Children's Hospital, Athens, Greece
,
Alexandra Stamoulakatou Hematology Laboratory, “Aghia Sophia” Children's Hospital, Athens, Greece
,
Dimitra Liapi Hematology Laboratory, Venizelio-Pananio General Hospital, Heraklion, Greece
,
Dimitrios Kampourakis Pediatric Clinic, Agios Nikolaos General Hospital, Agios Nikolaos, Greece
,
Amalia Tsilimigaki Second Pediatric Clinic, Venizelio-Pananio General Hospital, Heraklion, Greece
,
Emmanuel Kanavakis Department of Medical Genetics, University of Athens, “Aghia Sophia” Children's Hospital, Athens, Greece
&
Joanne Traeger-Synodinos Department of Medical Genetics, University of Athens, “Aghia Sophia” Children's Hospital, Athens, GreeceCorrespondence[email protected]
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Pages 379-385 | Received 24 Jan 2008, Accepted 01 Feb 2008, Published online: 07 Jul 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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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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Articles from other publishers (3)

Berndt Zur. (2016) Hemoglobin variants – pathomechanism, symptoms and diagnosis. LaboratoriumsMedizin 39:s1.
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Berndt Zur. (2015) Hämoglobinvarianten – Pathomechanismus, Symptome und Diagnostik. LaboratoriumsMedizin 39:5, pages 311-324.
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Yen-Hui Chiu, Ying-Chen Chang, Yu-Hsin Chang, Dau-Ming Niu, Yan-Ling Yang, Jun Ye, Jianhui Jiang, Yoshiyuki Okano, Dong Hwan Lee, Suthipong Pangkanon, Chulaluck Kuptanon, Ngu Lock Hock, Mary Anne Chiong, Barbra V Cavan, Kwang-Jen Hsiao & Tze-Tze Liu. (2012) Mutation spectrum of and founder effects affecting the PTS gene in East Asian populations. Journal of Human Genetics 57:2, pages 145-152.
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