Analysis Of δ-Globin Gene Mutations in the Chinese Population
Author:
Publisher
Informa UK Limited
Subject
Biochemistry, medical,Clinical Biochemistry,Genetics(clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.3109/03630269.2012.747965
Reference22 articles.
1. Co-Inheritance of β- and δ-Thalassemia Compromising Prenatal Screening in a Chinese Couple Seeking Prevention
2. The prevalence and spectrum of and thalassaemia in Guangdong Province: implications for the future health burden and population screening
3. Delta-thalassemia caused by disruption of the site for an erythroid- specific transcription factor, GATA-1, in the delta-globin gene promoter
4. Mutation at −30 (T→C) of the δ‐Globin Gene in a Taiwanese β‐Thalassemia Carrier
5. Identification of four novel delta-globin gene mutations in Greek Cypriots using polymerase chain reaction and automated fluorescence- based DNA sequence analysis
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1. Mutational spectrum of HBD gene in the Chinese population: Description of 36 mutations including 11 novel variants;International Journal of Laboratory Hematology;2023-08-22
2. Prospective screening for δ-hemoglobinopathies associated with decreased hemoglobin A2 levels or hemoglobin A2 variants: A single center experience;Clinica Chimica Acta;2023-07
3. Identification of rare thalassemia variants using third-generation sequencing;Frontiers in Genetics;2023-01-04
4. A New Mutation, Hb A2-Canakkale [δ10(A7)Ala→Val; HBD: c.32C>T], and Other Well-Known δ Variants Identified in a Selected Cohort with Low Hb A2 Levels;Hemoglobin;2022-03-04
5. An Evaluation for the Causes of Reduced Hb A2 and the Molecular Characterization of HBD Variants in Hong Kong;Hemoglobin;2021-11-02
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