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Keyword [α thalassemia]
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1. Initation Coden Mutation Of α2-Globin Gene Causing α-Thalassemia
2. Study For Homozygous ~Gγ-158C→T Mutation Resulting In Non-Deletional Hereditary Persistence Of Fetal Hemoglobin And Compounded With Thalassemia
3. Molecular Characterization And Gene Mutation Spectrum Of Thalassemia In Fuzhou Area,Fujian Province China
4. Establishment And Clinical Evaluation Of Melting Analysis Testing System For Deletional α-thalassemia
5. Identification Of Two Novel Large Segmental Deletion Involving α-globin Gene Cluster Causing Thalassemia
6. The Genotypes Research On α-thalassimia In Zhanjiangn Area Guangdong Province
7. Molecular Genetic Analysis Of Rare Thalassemia In Three Chinese Families
8. Molecular Detection Of Spinal Muscular Atrophy By MALDI-TOF MS&Preimplantation Genetic Diagnosis Of α-thalassemia SEA Deletion Utilizing Whole Genome Amplification And Short Fragment Gap-PCR Method
9. The Application Of Triple TaqMan Real-time Fluorescence Quantitative PCR In The Clinical Diagnosis Of Deletion α-thalassemia
10. A Genetic Study Of Surviving Patient With Hb Bart’s Hydrops Fetalis Syndrome Due To High Expression Of ζ-globin
11. Microecological Risk Assessment Of Pregnant Women With Mild Thalassemia Based On Intestinal Metagenomics
12. Research On Quality Control Products For α-thalassemia Gene Mutation Detection Based On CRISPR/Cas9 Technology
13. Micro-132-3p Regulates Oxidative Stress By Targeting FOXO3 In H-Constant Spring α-thalassemia
14. The Study On α-Thalassemia Hemoglobin H Disease
15. Research Of Pedigree-independent Haplotype Construction For Preimplantation Genetic Testing In Southeast Asian Deletion α-thalassemia
16. A Novel Mutation In ATRX Causes Alpha-Thalassemia X-Linked Intellectual Disability Syndrome In A Han Chinese Family
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