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Hemoglobin
international journal for hemoglobin research
Volume 34, 2010 - Issue 5
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Original Article

Variable and Often Severe Phenotypic Expression in Patients with the α-Thalassemic Variant Hb Agrinio [α29(B10)Leu→Pro (α2)]

Joanne Traeger-Synodinos Medical Genetics, Athens University Medical School, “Aghia Sophia” Children's Hospital, Athens, GreeceCorrespondence[email protected]
,
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
,
Alexandra Stamoulakatou Hematology Laboratory, “Aghia Sophia” Children's Hospital, Athens, Greece
,
Vasilis Ladis Thalassemia Unit, First Department of Pediatrics, Athens University Medical School, “Aghia Sophia” Children's Hospital, Athens, Greece
,
Tania Siahanidou Neonatal Unit, First Department of Pediatrics, Athens University Medical School, “Aghia Sophia” Children's Hospital, Athens, Greece
,
Irine Fylaktou Medical Genetics, Athens University Medical School, “Aghia Sophia” Children's Hospital, Athens, Greece
&
Emmanuel Kanavakis Medical Genetics, Athens University Medical School, “Aghia Sophia” Children's Hospital, Athens, Greece
 show all
Pages 430-438 | Received 31 Mar 2010, Accepted 20 Apr 2010, Published online: 20 Sep 2010

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Marija Dimishkovska, Maja Kuzmanovska, Svetlana Kocheva, Kata Martinova, Oliver Karanfilski, Zlate Stojanoski & Dijana Plaseska-Karanfilska. (2017) First Cases of Hb Agrinio Described in Patients from the Republic of Macedonia. Hemoglobin 41:4-6, pages 308-310.
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Antonis Kattamis, Polyxeni Delaporta, Irene Fylaktou, Christina Vrettou, Dimitra Kyriakopoulou, Alexandra Stamoulakatou, Ioannis Papassotiriou, Emmanuel Kanavakis & Jan Traeger-Synodinos. (2015) Hb Souli, a 6 bp In-Frame Deletion on the HBA2 Gene (HBA2: c.[41-46delCCTGGG]) Leads to α-Thalassemia Intermedia, When in Trans to a Single α-Globin Gene Deletion. Hemoglobin 39:1, pages 55-57.
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Felix de la Fuente-Gonzalo, Montserrat Baiget, Isabel Badell, Pilar Ricard, Lara Vinuesa, Jorge Martínez-Nieto, Paloma Ropero, Ana Villegas, Fernando A. González, Joaquin Díaz-Mediavilla & The Erythropathology Spanish Group. (2012) Study of Three Families with Hb Agrinio [α29(B10)Leu→Pro, CTG>CCG (α2)] in the Spanish Population: Three Homozygous Cases. Hemoglobin 36:6, pages 526-532.
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Maria Elisabetta Paglietti, Maria Carla Sollaino, Daniela Loi, Susanna Barella, Maria Franca Desogus & Renzo Galanello. (2012) First Detection of Hb Taybe [α38(C3) or α39(C4) Thr→0 (α1)] in An Italian Child. Hemoglobin 36:3, pages 299-304.
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Articles from other publishers (4)

Michael D. Diamantidis, Stefania Pitsava, Omar Zayed, Ioanna Argyrakouli, Konstantinos Karapiperis, Christos Chatzoulis, Evangelos Alexiou, Achilles Manafas, Evangelos Tsangalas & Konstantinos Karakoussis. (2023) Concomitant Presence of Hb Agrinio and - -Med Deletion in a Greek Male Patient with Hemoglobinopathy H: More Severe Phenotype and Literature Review. Hematology Reports 15:3, pages 483-490.
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Sarah Szepetowski, Claire Berger, Philippe Joly, Sandrine Baron‐Joly, Yoann Huguenin, Aurélie Cantais, Sophie Brun, Cécile Ged, Catherine Badens, Isabelle Thuret, Muriel Giansily‐Blaizot, Serge Pissard & Patricia Aguilar‐Martinez. (2022) Homozygosity for the hyperunstable hemoglobin variant Hb Agrinio ( HBA2 :c. 89T >C) leads to severe antenatal anemia: Eight new cases in three families . American Journal of Hematology 97:11.
Crossref
Barbara J. Bain. 2020. Haemoglobinopathy Diagnosis. Haemoglobinopathy Diagnosis 85 184 .
Margarita Petropoulou, Amalia Poula, Jan Traeger-Synodinos, Emmanuel Kanavakis, Theodore K. Christopoulos & Penelope C. Ioannou. (2015) Multi-allele DNA biosensor for the rapid genotyping of ‘nondeletion’ alpha thalassaemia mutations in HBA1 and HBA2 genes by means of multiplex primer extension reaction. Clinica Chimica Acta 446, pages 241-247.
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