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Hemoglobin
international journal for hemoglobin research
Volume 39, 2015 - Issue 4
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Original Article

Compound Heterozygosity for HKαα and an in Cis Deletion of Double α Genes Presents as α-Thalassemia Trait

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Pages 256-259 | Received 10 Oct 2014, Accepted 11 Nov 2014, Published online: 27 May 2015

Keep up to date with the latest research on this topic with citation updates for this article.

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Manna Sun, Jiwu Lou, Ying Zhag, Youqing Fu, Yunshi Dai & Yanhui Liu. (2019) Polymorphisms of α-Globin Genes Compromise Polymerase Chain Reaction-Based α-Thalassemia Genotyping in Three Chinese Families. Hemoglobin 43:2, pages 101-106.
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Articles from other publishers (3)

Ju Long & Enqi Liu. (2021) The carriage rates of αααanti3.7, αααanti4.2, and HKαα in the population of Guangxi, China measured using a rapid detection qPCR system to determine CNV in the α-globin gene cluster. Gene 768, pages 145296.
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Wenjuan Wang, Haiqing Zheng, Dan Zeng, Linbin Jiang, Donglan Yu, Yuzhong Yang, Qiao Feng, Yang Xia & Chunjiang Zhu. (2020) The pedigree analysis and prenatal diagnosis of Hong Kongαα Thalassemia and the sequence analysis of Hong Kongαα Allele . Molecular Genetics & Genomic Medicine 8:7.
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Man-Yu Wu, Jian-Ying Zhou, Jian Li & Dong-Zhi Li. (2015) The Frequency of α-Globin Gene Triplication in a Southern Chinese Population. Indian Journal of Hematology and Blood Transfusion 32:S1, pages 320-322.
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