Compound Heterozygosity for HKααand anin CisDeletion of DoubleαGenes Presents asα-Thalassemia Trait
Author:
Publisher
Informa UK Limited
Subject
Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.3109/03630269.2015.1039026
Reference16 articles.
1. Nonimmune Hydrops Fetalis Diagnosed during the Second Half of Pregnancy in Southern China
2. Hemoglobin H disease: not necessarily a benign disorder
3. The prevalence and spectrum of and thalassaemia in Guangdong Province: implications for the future health burden and population screening
4. Unusual Rearrangement of the α-Globin Gene Cluster Containing Both the −α3.7 and αααanti-4.2 Crossover Junctions: Clinical Diagnostic Implications and Possible Mechanisms
5. Molecular characterization and clinical presentation of HKαα and anti-HKαα alleles in southern Chinese subjects
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1. Accurate genotype diagnosis of Hong Kongαα thalassemia based on third-generation sequencing;Annals of Translational Medicine;2022-10
2. 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;2021-02
3. The pedigree analysis and prenatal diagnosis of Hong Kongαα Thalassemia and the sequence analysis of Hong Kongαα Allele;Molecular Genetics & Genomic Medicine;2020-05-18
4. Polymorphisms of α-Globin Genes Compromise Polymerase Chain Reaction-Based α-Thalassemia Genotyping in Three Chinese Families;Hemoglobin;2019-03-04
5. The Frequency of α-Globin Gene Triplication in a Southern Chinese Population;Indian Journal of Hematology and Blood Transfusion;2015-09-02
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