Identification of double heterozygous -α <sup>4.2Ⅰ</sup> /-α <sup>4.2Ⅱ</sup> using third-generation sequencing-Reference-Cited by-同舟云学术

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Identification of double heterozygous -α ^4.2Ⅰ /-α ^4.2Ⅱ using third-generation sequencing

Published:2023-08-24 Issue:1 Volume:28 Page:
ISSN:1607-8454
Container-title:Hematology
language:en
Short-container-title:Hematology

Author:

Liang Liang¹,Xiao Yongjun²,Guo Weilin³,Xie Tiantian⁴,Zheng Lihong¹,Li Youqiong¹^ORCID

Affiliation:

1. Center for Medical Genetics and Prenatal Diagnosis, People’s Hospital of Guangxi Zhuang Autonomous Region, Nanning, People’s Republic of China

2. Department of clinical laboratory, The Second Nanning People’s Hospital of Guangxi Zhuang Autonomous Region, Nanning, People’s Republic of China

3. Yaneng Biotechnology Corporation, Shenzhen, People’s Republic of China

4. Berry Genomics Corporation, Beijing, People’s Republic of China

Funder

Natural Science Foundation of Guangxi

Health Department Research Fund of Guangxi

Publisher

Informa UK Limited

Subject

Hematology,Hematology

Link

https://www.tandfonline.com/doi/pdf/10.1080/16078454.2023.2250646

Reference12 articles.

1. Molecular Basis and Genetic Modifiers of Thalassemia

2. Thalassaemia

3. Molecular epidemiological survey of haemoglobinopathies in the Guangxi Zhuang Autonomous Region of southern China

4. Molecular characteristics of α+-thalassemia (3.7 kb deletion) in Southeast Asia: Molecular subtypes, haplotypic heterogeneity, multiple founder effects and laboratory diagnostics

5. The -α^3.7III subtype of α⁺-thalassemia was identified in China

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1. Asymptomatic Co-Inheritance of Hb Leiden (HBB:c.22_24delGAG), Hb Q-Thailand (HBA1:c.223G > C) and Deletional Alpha Thalassemia in a Young Chinese Male;Indian Journal of Hematology and Blood Transfusion;2024-05-16

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