Citations (21)
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Taner Karakaya, Fatma Silan & Ozturk Ozdemir. (2022) A New Mutation, Hb A2-Canakkale [δ10(A7)Ala→Val; HBD: c.32C>T], and Other Well-Known δ Variants Identified in a Selected Cohort with Low Hb A2 Levels. Hemoglobin 46:2, pages 87-90.
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Nelson C. N. Chan, Terry H. Y. Wong, Kelvin C. K. Cheng, Natalie P. H. Chan & Margaret H. L. Ng. (2021) An Evaluation for the Causes of Reduced Hb A2 and the Molecular Characterization of HBD Variants in Hong Kong. Hemoglobin 45:6, pages 387-391.
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Hai-Shen Tang, De-Gang Wang, Lv-Yin Huang & Dong-Zhi Li. (2018) δ-Thalassemia with Complete Absence of Hb A2 in a Chinese Family. Hemoglobin 42:2, pages 135-137.
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Manna Sun, Jiwu Lou, Ying Zhao & Yanhui Liu. (2018) Molecular and Hematological Characterization of Two Novel δ-Globin Gene Mutations Found in Chinese Individuals. Hemoglobin 42:2, pages 132-134.
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Gui-Lan Chen, Lv-Yin Huang, Jian-Ying Zhou & Dong-Zhi Li. (2017) Hb A2-Tianhe (HBD: c.323G>A): First Report in a Chinese Family with Normal Hb A2-β-Thalassemia Trait. Hemoglobin 41:4-6, pages 291-292.
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Jin-Mei Yan, Jian-Ying Zhou, Xing-Mei Xie, Jian Li & Dong-Zhi Li. (2016) A New δ-Globin Gene Variant: Hb A2-Fengshun [δ121(GH4)Glu→Lys (HBD: c.364G > A)]. Hemoglobin 40:3, pages 213-214.
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Articles from other publishers (15)
Anping Xu, Mingyang Li, Yinghui Ye, Liping Li, Minjing Ma, Shang Ying Wu & Ling Ji. (2023)
Mutational spectrum of
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. International Journal of Laboratory Hematology 45:6, pages 961-968.
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Chulikon Hanart, Kritsada Singha, Yotsombat Changtrakul, Supan Fucharoen & Hataichanok Srivorakun. (2023) Prospective screening for δ-hemoglobinopathies associated with decreased hemoglobin A2 levels or hemoglobin A2 variants: A single center experience. Clinica Chimica Acta 547, pages 117417.
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Qin Liu, Qianting Chen, Zonglei Zhang, Shiyi Peng, Jing Liu, Jialun Pang, Zhengjun Jia, Hui Xi, Jiaqi Li, Libao Chen, Yinyin Liu & Ying Peng. (2023) Identification of rare thalassemia variants using third-generation sequencing. Frontiers in Genetics 13.
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Keivan Moradi, Aboozar Mohammadi & Mohsen Kazeminia. (2021) In silico prediction of HBD gene variants in the Iranian population. Egyptian Journal of Medical Human Genetics 22:1.
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Jianlong Zhuang, Na Zhang, Yuanbai Wang, Hegan Zhang, Yu Zheng, Yuying Jiang, Yingjun Xie & Dongmei Chen. (2021) Molecular Characterization Analysis of Thalassemia and Hemoglobinopathy in Quanzhou, Southeast China: A Large-Scale Retrospective Study. Frontiers in Genetics 12.
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Kritsada Singha, Goonnapa Fucharoen & Supan Fucharoen. (2021) δ-Hemoglobinopathies in Thailand: screening, molecular basis, genotype-phenotype interaction, and implication for prevention and control of thalassemia. Annals of Hematology 100:8, pages 1953-1963.
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Meihuan Chen, Hailong Huang, Lingji Chen, Na Lin, Min Zhang, Yuan Lin & Liangpu Xu. (2020) First report of the spectrum of δ‐globin gene mutations among women of reproductive age in Fujian area—Discrimination of δ‐thalassemia, α‐thalassemia, and Iron Deficiency Anemia. Journal of Clinical Laboratory Analysis 34:11.
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Youqiong Li, Tongfeng Huang, Tian Mao, Xiuqun Zhang, Liang Liang & Menghui Meng. (2020)
Detection of a Hb A
2
‐Melbourne (HBD: c.130G>A) combined with β‐thalassemia in a Chinese individual
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Ahmad Shoujaa, Yasser Mukhalalaty, Hossam Murad & Faizeh Al-Quobaili. (2020) A First Case of Hemoglobin Castilla [Beta 32(B14) Leu>Arg; HBB: c.98T>G] Associated with [IVS-I-1 (G>A); HBB:c.92+1G>A] Mutation Found in a Syrian Betathalassemia Patient. Thalassemia Reports 10:1, pages 8396.
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Faten Moassas, Mohamad Sayah Nweder & Hossam Murad. (2019) Hb Knossos (HBB: c.82G > T), β-globin CD 5 (−CT) (HBB: c.17_18delCT) and δ-globin CD 59 (−a) (HBD: c.179delA) mutations in a Syrian patient with β-thalassemia intermedia. BMC Pediatrics 19:1.
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Jie Zhang, Peng Li, Yang Yang, Yuanlong Yan, Xiaohong Zeng, Dongmei Li, Hong Chen, Jie Su & Baosheng Zhu. (2019) Molecular epidemiology, pathogenicity, and structural analysis of haemoglobin variants in the Yunnan province population of Southwestern China. Scientific Reports 9:1.
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Jie Zhang, Yang Yang, Peng Li, Yuanlong Yan, Tao Lv, Tingting Zhao, Xiaohong Zeng, Dongmei Li, Xiaoyan Zhou, Hong Chen, Jie Su, Tonghua Yang, Jing He & Baosheng Zhu. (2019) Analysis of deletional hereditary persistence of fetal hemoglobin/δβ‐thalassemia and δ‐globin gene mutations in Southerwestern China. Molecular Genetics & Genomic Medicine 7:6.
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Phumin Chaweephisal, Arunee Phusua, Kanda Fanhchaksai, Supatra Sirichotiyakul & Pimlak Charoenkwan. (2019) Borderline hemoglobin A2 levels in northern Thai population: HBB genotypes and effects of coinherited alpha-thalassemia. Blood Cells, Molecules, and Diseases 74, pages 13-17.
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Shuichi Otabe, Hitomi Nakayama, Tsuyoshi Ohki, Eri Soejima, Yuji Tajiri & Kentaro Yamada. (2016) Haemoglobin variants may cause significant differences in haemoglobin A1c as measured by high-performance liquid chromatography and enzymatic methods in diabetic patients: a cross-sectional study. Annals of Clinical Biochemistry: International Journal of Laboratory Medicine 54:4, pages 432-437.
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Ji-Wu Lou, Dong-Zhi Li, Yu Zhang, Yi He, Man-Na Sun, Wan-Ling Ye & Yan-Hui Liu. (2014) Delineation of the molecular basis of borderline hemoglobin A2 in Chinese individuals. Blood Cells, Molecules, and Diseases 53:4, pages 261-264.
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