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Hemoglobin
international journal for hemoglobin research
Volume 43, 2019 - Issue 4-5
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A β-Thalassemia Trait with Two Mutations in Cis in a Chinese Family

Jian LiPrenatal Diagnostic Center, Guangzhou Women and Children’s Medical Center, Guangzhou Medical University, Guangzhou, People’s Republic of ChinaView further author information
,
Fan JiangPrenatal Diagnostic Center, Guangzhou Women and Children’s Medical Center, Guangzhou Medical University, Guangzhou, People’s Republic of ChinaView further author information
,
Li ZhenPrenatal Diagnostic Center, Guangzhou Women and Children’s Medical Center, Guangzhou Medical University, Guangzhou, People’s Republic of ChinaView further author information
,
Xue-Wei TangPrenatal Diagnostic Center, Guangzhou Women and Children’s Medical Center, Guangzhou Medical University, Guangzhou, People’s Republic of ChinaView further author information
&
Dong-Zhi LiPrenatal Diagnostic Center, Guangzhou Women and Children’s Medical Center, Guangzhou Medical University, Guangzhou, People’s Republic of ChinaCorrespondence[email protected]
View further author information
Pages 289-291 | Received 02 Aug 2019, Accepted 18 Oct 2019, Published online: 05 Nov 2019

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Danqing Qin, Jicheng Wang, Cuize Yao, Xiuqin Bao, Jie Liang & Li Du. (2023) Hb Q-Thailand heterozygosity unlinked with the (–α4.2/) α+-thalassemia deletion allele identified by long-read SMRT sequencing: hematological and molecular analyses. Hematology 28:1.
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Juan Liao, Qin Li, Li-Qin Ling, Chao-Nan Liu, Xun-Bei Huang & Jing Zhou. (2022) A Triple-Heterozygous β-Thalassemia Patient Demonstrated an Unusual Electrophoresis Pattern Due to a Novel β0 Mutation [an IVS-II-654 (C>T) mutation with a Hb Zürich-Langstrasse (HBB: c.151A>T) mutation in cis]. Hemoglobin 46:4, pages 249-252.
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