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Bo-Dan Wu, Xiao-Yan Zhou, Mei-Juan Xie, Chan-Chan Jin, Yuan-Long Yan, Jing He, Bao-Sheng Zhu & Jie Zhang. (2023) Identification of a Novel 7-bp Deletion in the α-Globin Gene Cluster in One Chinese Family. Hemoglobin 47:2, pages 49-51.
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Xiao-Hong He, Rui Zhang, Guang-Xing Mai, Li-Rong Ren & Dong-Zhi Li. (2018) First Report of a Case with Nondeletional Hb H Disease Caused by IVS-I-116 (A>G) of the α2-Globin Gene. Hemoglobin 42:5-6, pages 344-346.
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Samaneh Farashi, Shadi Vakili, Negin F. Garous, Mehri Ashki, Fatemeh Forouzesh Pour, Fatemeh Zeinali, Fariba Rad, Hashem Imanian, Azita Azarkeivan & Hossein Najmabadi. (2016) Identification of Mutations Causing Aberrant Termination and Deficient Splice Donor Site on the HBA1 Gene. Hemoglobin 40:1, pages 38-43.
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Samaneh Farashi, Nooshin Bayat, Shadi Vakili, Negin Faramarzi Garous, Mehri Ashki, Hashem Imanian, Hossein Najmabadi & Azita Azarkeivan. (2016) Point mutations which should not be overlooked in Hb H disease. Expert Review of Hematology 9:1, pages 107-113.
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Samaneh Farashi, Shadi Vakili, Negin F. Garous, Mehri Ashki, Hashem Imanian, Azita Azarkeivan & Hossein Najmabadi. (2015) Mutations on the α2-Globin Gene That May Trigger α+-Thalassemia. Hemoglobin 39:6, pages 398-402.
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Nima Hafezi-Nejad, Mohsen Khosravi, Nooshin Bayat, Ariana Kariminejad, Valeh Hadavi, Christian Oberkanins, Azita Azarkeivan & Hossein Najmabadi. (2014) Characterizing a Cohort of α-Thalassemia Couples Collected During Screening for Hemoglobinopathies: 14 Years of an Iranian Experience. Hemoglobin 38:3, pages 153-157.
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