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Hemoglobin
international journal for hemoglobin research
Volume 39, 2015 - Issue 6
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Short Communication

First Description of a β-Thalassemia Mutation, −86 (C > G) (HBB: c.−136C > G), in a Chinese Family

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Pages 448-450 | Received 24 Apr 2015, Accepted 15 May 2015, Published online: 13 Aug 2015

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Hossam Murad, Faten Moasses, Amir Dabboul, Yasser Mukhalalaty, Ahmad Omar Bakoor, Walid Al-Achkar & Rami A. Jarjour. (2018) Geographical distribution of β-globin gene mutations in Syria. Hematology 23:9, pages 697-704.
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Faten Moassas, Ayman Alabloog & Hossam Murad. (2018) Description of a Rare β-Globin Gene Mutation: –86 (C>G) (HBB: c.-136C>G) Observed in a Syrian Family. Hemoglobin 42:3, pages 203-205.
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Worrawalan Lerttham, Goonnapa Fucharoen, Supawadee Yamsri & Supan Fucharoen. (2015) Two Independent Genetic Origins of β+- Thalassemia Due to -31 A to G Mutation in Thai and Japanese Populations. International Journal of Human Genetics 15:4, pages 191-198.
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Articles from other publishers (1)

Sheng He, Qian Qin, Shang Yi, Yuan Wei, Li Lin, Shaoke Chen, Jianping Deng, Xianmin Xu, Chenguang Zheng & Biyan Chen. (2017) Prevalence and genetic analysis of α- and β-thalassemia in Baise region, a multi-ethnic region in southern China. Gene 619, pages 71-75.
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