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Azam Azimi, Susan Tahmasebi, Keivan Moradi, Parham Nejati & Reza Alibakhshi. (2020) Severe α-Thalassemia Due to Compound Heterozygosity for Hb Adana (α59 Gly>Asp) (HBA1: c.179G > A) and Codon 127 (A > T) (HBA2: c.382A > T) in an Iranian Family. Hemoglobin 44:2, pages 139-142.
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Stamatia Theodoridou, Aikaterini Teli, Eleni Yfanti, Timoleon-Achilleas Vyzantiadis, Theodoros Theodoridis & Marina Economou. (2018) Compound Heterozygosity for Hb Adana (HBA2: c.179G>A) and the –α3.7/αα Thalassemia Deletion in Greece: Clinical Phenotype and Genetic Counseling. Hemoglobin 42:2, pages 129-131.
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Tekin Aksu, Neşe Yaralı, Cengiz Bayram, Ali Fettah, Zekai Avcı & Bahattin Tunç. (2014) Homozygosity for HBA1: c.179G > A: Hb Adana in an Infant. Hemoglobin 38:6, pages 449-450.
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Articles from other publishers (3)
Divashini Vijian, Wan Suriana Wan Ab Rahman, Kannan Thirumulu Ponnuraj & Zefarina Zulkafli. (2022) Clinical and Haematological Parameters of Commonly Reported Non-deletional α-thalassaemia Mutations in Southeast Asia: A Review. Malaysian Journal of Medicine and Health Sciences 18:5, pages 190-199.
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Sharon A. Singh, Susmita Sarangi, Abena Appiah-Kubi, Peihong Hsu, W. Byron Smith, Patrick G. Gallagher, Bertil Glader & David H. K. Chui. (2018) Hb Adana (HBA2 or HBA1: c.179G > A) and alpha thalassemia: Genotype-phenotype correlation. Pediatric Blood & Cancer 65:9, pages e27220.
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Samaneh Farashi & Cornelis L. Harteveld. (2018) Molecular basis of α-thalassemia. Blood Cells, Molecules, and Diseases 70, pages 43-53.
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