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Hemoglobin
international journal for hemoglobin research
Volume 42, 2018 - Issue 5-6
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Original Article

Results of Coexistence of β-Thalassemia Minor in Hb H Disease Patients

Gui-Lan ChenPrenatal Diagnostic Center, Guangzhou Women and Children’s Medical Center affiliated to Guangzhou Medical University, Guangzhou, Guangdong Province, People’s Republic of ChinaView further author information
,
Fan JiangPrenatal Diagnostic Center, Guangzhou Women and Children’s Medical Center affiliated to Guangzhou Medical University, Guangzhou, Guangdong Province, People’s Republic of ChinaView further author information
,
Jian LiPrenatal Diagnostic Center, Guangzhou Women and Children’s Medical Center affiliated to Guangzhou Medical University, Guangzhou, Guangdong Province, People’s Republic of ChinaView further author information
,
Jian-Ying ZhouPrenatal Diagnostic Center, Guangzhou Women and Children’s Medical Center affiliated to Guangzhou Medical University, Guangzhou, Guangdong Province, People’s Republic of ChinaView further author information
&
Dong-Zhi LiPrenatal Diagnostic Center, Guangzhou Women and Children’s Medical Center affiliated to Guangzhou Medical University, Guangzhou, Guangdong Province, People’s Republic of ChinaCorrespondence[email protected]
View further author information
Pages 306-309 | Received 26 Oct 2018, Accepted 09 Dec 2018, Published online: 07 Jan 2019

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Yuling Qiu, Shilu Wei, Wei Hou, Ketong Lai, Hengying Zhu, Wenwei Li, Qi Li, Zheng Yang, Qisheng Shu, Ping Chen & Wuning Mo. (2023) Molecular Basis and Hematologic Phenotype of Hemoglobin H Disease Combined with Two Rare β-Globin Mutations. Hemoglobin 47:2, pages 52-55.
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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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Articles from other publishers (2)

Hou Qian, Jianlin Huang, Ji Xu, Weihua Zhao, Xiufeng Ye & Wenlan Liu. (2020) Prenatal diagnosis of a rare β ‐thalassemia gene －90 (C>T) ( HBB : c.‐140 C>T) mutation associated with deletional Hb H disease (‐‐ SEA /‐ α 4.2 ) . Molecular Genetics & Genomic Medicine 8:11.
Crossref
Barbara J. Bain. 2020. Haemoglobinopathy Diagnosis. Haemoglobinopathy Diagnosis 85 184 .

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