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Hemoglobin
international journal for hemoglobin research
Volume 40, 2016 - Issue 3
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Short Communication

First Case of a Compound Heterozygosity for Two Nondeletional α-Thalassemia mutations, Hb Constant Spring and Hb Quong Sze

Jian-Ying ZhouPrenatal Diagnostic Center, Guangzhou Women & Children Medical Center affiliated to Guangzhou Medical University, Guangzhou, Guangdong, People’s Republic of China
,
Jin-Mei YanPrenatal Diagnostic Center, Guangzhou Women & Children Medical Center affiliated to Guangzhou Medical University, Guangzhou, Guangdong, People’s Republic of China
,
Jian LiPrenatal Diagnostic Center, Guangzhou Women & Children Medical Center affiliated to Guangzhou Medical University, Guangzhou, Guangdong, People’s Republic of China
&
Dong-Zhi LiPrenatal Diagnostic Center, Guangzhou Women & Children Medical Center affiliated to Guangzhou Medical University, Guangzhou, Guangdong, People’s Republic of ChinaCorrespondence[email protected]
Pages 210-212 | Received 12 Dec 2015, Accepted 15 Jan 2016, Published online: 09 Mar 2016

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Li Liu, Yan Sun, Shiping Chen, Churen Yu, Peijie Cao, Jun Sun, Zhiyu Peng & Ping Mao. (2021) Identification of Two Novel Thalassemia Variants, HBA1: c.263delA and HBA2: c.376dupC, in Chinese Individuals. Hemoglobin 45:1, pages 49-51.
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Yuan Liang, Qi Peng, Miao Li, Siping Li, Wenrui Li & Xiaomei Lu. (2017) A Novel α-Thalassemia Nonsense Mutation on the α2-Globin Gene: HBA2: c.184A>T. Hemoglobin 41:4-6, pages 306-307.
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