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Hafiza Alauddin, Khairina Kamarudin, Tang Yee Loong, Raja Zahratul Azma, Azlin Ithnin, Norunaluwar Jalil, Noor-Farisah Razak, Danny Koh-Xuan-Rong, Endom Ismail, Loh C-Khai, Zarina Abdul Latiff, Hamidah Alias & Ainoon Othman. (2018) A Unique Interaction of IVS-I-1 (G>A) (HBA2: c.95+1G>A) with Hb Adana (HBA2: c.179G>A) Presenting as Transfusion-Dependent α-Thalassemia. Hemoglobin 42:4, pages 247-251.
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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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Hua Jiang, Lv-Yin Huang, Li Zhen, Fan Jiang & Dong-Zhi Li. (2017) Two α1-Globin Gene Point Mutations Causing Severe Hb H Disease. Hemoglobin 41:4-6, pages 293-296.
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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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Hafiza Alauddin, Noor-Adilah Jaapar, Raja Z. Azma, Azlin Ithnin, Noor-Farisah A. Razak, C-Khai Loh, Hamidah Alias, Zarina Abdul-Latiff & Ainoon Othman. (2014) A Case Series of α-Thalassemia Intermedia Due to Compound Heterozygosity for Hb Adana [HBA2: c179G>A (or HBA1); p.Gly60Asp] With Other α-Thalassemias in Malay Families. Hemoglobin 38:4, pages 277-281.
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Dewi Megawati, Ita M. Nainggolan, Maria Swastika, Susi Susanah, Johanes C. Mose, Alida R. Harahap & Iswari Setianingsih. (2014) Severe α-Thalassemia Intermedia Due to a Compound Heterozygosity for the Highly Unstable Hb Adana (HBA2: c.179G>A) and a Novel Codon 24 (HBA2: c.75T>A) Mutation. Hemoglobin 38:2, pages 149-151.
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Jianpei Fang, Luming Chen, Ruiping Zeng, Qiuhong Tian, Weiying Jiang, Hongyi Li, Zheng Chen, Chuanshu Du & Suqin Chen. (2014) The Hb H Disease Genotypes in Southern China. Hemoglobin 38:1, pages 76-78.
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Ita M. Nainggolan, Alida Harahap, Debby D. Ambarwati, Rosalina V. Liliani, Dewi Megawati, Maria Swastika & Iswari Setianingsih. (2013) Interaction of Hb Adana (HBA2: c.179G>A) with Deletional and Nondeletional α+-Thalassemia Mutations: Diverse Hematological and Clinical Features. Hemoglobin 37:3, pages 297-305.
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Articles from other publishers (9)
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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Herminio López-Escribano & Ausias Hervás-Romero. (2021) Study of alpha-thalassemia in the clinical laboratory: genotypes-phenotypes of clinical interest and their diagnostic approach. Revista de Medicina de Laboratorio.
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Barbara J. Bain. 2020. Haemoglobinopathy Diagnosis. Haemoglobinopathy Diagnosis
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Ahlem Achour, Elke Grouw, Femke Erp, Sandra Arkesteijn, Rianne Schaap, Jeanet ter Huurne, Sharda Bisoen, Maaike Verschuren & Cornelis L. Harteveld. (2019) The first report of hemoglobin E in combination with the highly unstable alpha‐globin variant Hb Adana: The importance of molecular confirmation. International Journal of Laboratory Hematology 41:3.
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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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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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Rahimah Ahmad, Mohamed Saleem, Nisha Aloysious, Punithawathy Yelumalai, Nurul Mohamed & Syahzuwan Hassan. (2013) Distribution of Alpha Thalassaemia Gene Variants in Diverse Ethnic Populations in Malaysia: Data from the Institute for Medical Research. International Journal of Molecular Sciences 14:9, pages 18599-18614.
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Barbara J. Bain. (2011) Haemoglobinopathy diagnosis: Algorithms, lessons and pitfalls. Blood Reviews 25:5, pages 205-213.
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