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Hemoglobin
international journal for hemoglobin research
Volume 44, 2020 - Issue 5
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Short Communications

Fifteen Cases of Hb J-Meerut: The Rare Association with Hb E and/or HBA1: c.-24C>G (or HBA2) Variants

Mohamed S.M. Khalila Department of Clinical Pathology, Faculty of Medicine, Assiut University, Assiut Governorate, EgyptCorrespondence[email protected]
ORCID Iconhttps://orcid.org/0000-0002-4117-4299View further author information
ORCID Icon,
Adele T. Timbsb National Haemoglobinopathy Reference Laboratory, Oxford Radcliffe Hospitals National Health Service Trust, Oxford, UKView further author information
,
Shirley J. Hendersonb National Haemoglobinopathy Reference Laboratory, Oxford Radcliffe Hospitals National Health Service Trust, Oxford, UKView further author information
,
Anna Schuhc Molecular Haematology, Molecular Diagnostics Centre and Department of Oncology, Churchill Hospital, Oxford, UKView further author information
&
John M. Oldb National Haemoglobinopathy Reference Laboratory, Oxford Radcliffe Hospitals National Health Service Trust, Oxford, UKView further author information
Pages 364-367 | Received 17 Jul 2020, Accepted 21 Aug 2020, Published online: 14 Sep 2020

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Maria Vousvouki, Evangelia-Eleni Delaki, Effrosyni Boutou, Eleni Yfanti, Genovefa Mantzou, Christina Karipidou, Athanasios Vyzantiadis, Athina Efstathiou, Maria Dimopoulou, Efthymia Vlachaki & Stamatia Theodoridou. (2024) A New α1-Globin Variant, Hb Ormylia [HBA1:c.63C > G; p.His21Gln]. Report of Eleven Cases in Northern Greece. Hemoglobin 48:2, pages 133-137.
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Wittaya Jomoui, Surada Satthakarn & Sitthichai Panyasai. (2023) Molecular understanding of unusual HbE-β+-thalassemia with Hb phenotype similar to HbE heterozygote: simple and rapid differentiation using HbE levels. Annals of Medicine 55:2.
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Mohamed S.M. Khalil, Adele T. Timbs, Shirley J. Henderson, Anna Schuh & John M. Old. (2020) Twelve Cases of Hb Manitoba [α102(G9)Ser→Arg]: the Fluctuation in the Variant Expression. Hemoglobin 44:6, pages 442-445.
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Articles from other publishers (1)

Jianlong Zhuang, Chunnuan Chen, Wanyu Fu, Yuanbai Wang, Qianmei Zhuang, Yulin Lu, Tiantian Xie, Ruofan Xu, Shuhong Zeng, Yuying Jiang, Yingjun Xie & Gaoxiong Wang. (2023) Third-Generation Sequencing as a New Comprehensive Technology for Identifying Rare α- and β-Globin Gene Variants in Thalassemia Alleles in the Chinese Population. Archives of Pathology & Laboratory Medicine 147:2, pages 208-214.
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