Citations (15)
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Abdul Aziz, Sudipta A. Das, Waqar A. Khan, Salma Sadiya, Bilquis Banu, Golam Sarwardi & Rowshon Z. Luna. (2017) A Novel β-Thalassemia Insertion/Frameshift Mutation Between Codons 77/78 (p.Leu78Profs*13 or HBB: c.235_236insC) Observed in a Family in Bangladesh. Hemoglobin 41:4-6, pages 311-313.
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Azita Zadeh-Vakili & Payman Eshghi. (2009) Detection of a Rare Mutation in An Iranian Family: Codons 37/38/39 (7 bp Deletion). Hemoglobin 33:6, pages 523-527.
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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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Ramachran V. Shaji, Alok Srivastava, Rajagopal Krishnamoorthy & Mammen Chandy. (2002) COEXISTENCE OF A NOVEL β-GLOBIN GENE DELETION (CODONS 81–87) WITH THE CODON 30 (G→C) MUTATION IN AN INDIAN PATIENT WITH β0-THALASSEMIA. Hemoglobin 26:3, pages 237-243.
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Ramachandran V. Shaji, Nathalie Gerard, Rajagopal Krishnamoorthy, Alok Srivastava & Mammen Chandy. (2002) A NOVEL β-THALASSEMIA MUTATION IN AN ASIAN INDIAN. Hemoglobin 26:1, pages 49-57.
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C. Vrettou, E. Kanavakis, J. Traeger-Synodinos, A. Metaxotou-Mavrommati, I. Basiakos, E. Maragoudaki, A. Stamoulakatou, I. Papassotiriou & C. Kattamis. (2000) Molecular Studies of β-Thalassemia Heterozygotes with Raised Hb F Levels. Hemoglobin 24:3, pages 203-220.
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J. Traeger-Synodinos, A. Metaxotou-Mavrommati, M. Karagiorga, C. Vrettou, I. Papassotiriou, A. Stamoulakatou & E. Kanavakis. (1999) Interaction of an α+-Thalassemia Deletion with Either a Highly Unstable α-Globin Variant (α2, Codon 59, GGC→GAC) or a Nondeletional α-Thalassemia Mutation (AATAA→AATAAG): Comparison of Phenotypes Illustrating “Dominant” α-Thalassemia. Hemoglobin 23:4, pages 325-337.
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Articles from other publishers (8)
Samaneh Farashi & Hossein Najmabadi. (2015) Diagnostic pitfalls of less well recognized HbH disease. Blood Cells, Molecules, and Diseases 55:4, pages 387-395.
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Rosa Santacroce, Antonia Ratti, Francesco Caroli, Barbara Foglieni, Alessandro Ferraris, Laura Cremonesi, Maurizio Margaglione, Marco Seri, Roberto Ravazzolo, Gabriella Restagno, Bruno Dallapiccola, Eric Rappaport, Eleanor S Pollak, Saul Surrey, Maurizio Ferrari & Paolo Fortina. (2002) Analysis of Clinically Relevant Single-Nucleotide Polymorphisms by Use of Microelectronic Array Technology. Clinical Chemistry 48:12, pages 2124-2130.
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David P. Steensma, James D. Hoyer & Virgil F. Fairbanks. (2001) Hereditary Red Blood Cell Disorders in Middle Eastern Patients. Mayo Clinic Proceedings 76:3, pages 285-293.
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Emmanuel Kanavakis, Ioannis Papassotiriou, Markissia Karagiorga, Christina Vrettou, Anna Metaxotou‐Mavrommati, Alexandra Stamoulakatou, Christos Kattamis & Joanne Traeger‐Synodinos. (2008) Phenotypic and molecular diversity of haemoglobin H disease: a Greek experience. British Journal of Haematology 111:3, pages 915-923.
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Emmanuel Kanavakis, Ioannis Papassotiriou, Markissia Karagiorga, Christina Vrettou, Anna Metaxotou-Mavrommati, Alexandra Stamoulakatou, Christos Kattamis & Joanne Traeger-Synodinos. (2000) Phenotypic and molecular diversity of haemoglobin H disease: a Greek experience. British Journal of Haematology 111:3, pages 915-923.
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Varda Oron-Karni, Dvora Filon, Yulia Shifrin, Elchanan Fried, Galina Pogrebijsky, Ariella Oppenheim & Deborah Rund. (2000) Diversity of ?-globin mutations and clinical presentation of ?-thalassemia in Israel. American Journal of Hematology 65:3, pages 196-203.
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Joanne Traeger-Synodinos, Ioannis Papassotiriou, Anna Metaxotou-Mavrommati, Christina Vrettou, Alexandra Stamoulakatou & Emmanuel Kanavakis. (2000) Distinct Phenotypic Expression Associated with a New Hyperunstable Alpha Globin Variant (Hb Heraklion, α1cd37(C2)Pro>0): Comparison to Other α-Thalassemic Hemoglobinopathies. Blood Cells, Molecules, and Diseases 26:4, pages 276-284.
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Xiao-Dong Huang, Xuexian O. Yang, Rui-Bin Huang, Hong-Yuan Zhang, Hua-Lu Zhao, Yan-Jun Zhao, Cheng-Le Huang, Chun-Jiang Hou & Jun-Wu Zhang. (2000) A novel four base-pair deletion within the A?-GLOBin gene promoter associated with slight increase of A? expression in adult. American Journal of Hematology 63:1, pages 16-19.
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