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Hemoglobin
international journal for hemoglobin research
Volume 46, 2022 - Issue 4
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Brief Report

Dominantly Inherited β-Thalassemia Caused by a Single Nucleotide Deletion in Exon 3 of the β-Globin Gene: Hb Xiangyang (HBB: c.393delT)

Xiao-Mei LinPrenatal 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
&
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 253-255 | Received 29 Dec 2021, Accepted 03 Feb 2022, Published online: 10 Jun 2022

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Ekaterina Demidova, Valentina Salomashkina, Daria Selivanova, Evgeny Litvin, Natalia Karamyan, Svetlana Mann, Valentina Dvirnyk, Salia Maryina, Natal’ya Petrova, Lana Gorgidze, Anastasiya Peredel’skaya, Nina Tsvetaeva, Nataliya Smetanina & Vadim Surin. (2023) Hb Ryazan: An Elongated C‐Terminal β-Chain Due to a New Frameshift Mutation, HBB: c.396delG p.Val133Trpfs*25. Hemoglobin 47:2, pages 97-101.
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