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Journal Abstract Search

156 related items for PubMed ID: 24826791

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  • 2. Molecular analysis and clinical significance of hemoglobin Quong Sze in Huizhou city, Southern China.
    Zhong Z, Guan Z, Chen D, Zhong G, He H, Yang K, Chen J.
    Taiwan J Obstet Gynecol; 2023 Sep; 62(5):709-712. PubMed ID: 37678999
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  • 4. First Case of a Compound Heterozygosity for Two Nondeletional α-Thalassemia mutations, Hb Constant Spring and Hb Quong Sze.
    Zhou JY, Yan JM, Li J, Li DZ.
    Hemoglobin; 2016 Jun; 40(3):210-2. PubMed ID: 26956449
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  • 11. The Hb E (HBB: c.79G>A), Mean Corpuscular Volume, Mean Corpuscular Hemoglobin Cutoff Points in Double Heterozygous Hb E/- -SEA α-Thalassemia-1 Carriers are Dependent on Hemoglobin Levels.
    Leckngam P, Limweeraprajak E, Kiewkarnkha T, Tatu T.
    Hemoglobin; 2017 Jan; 41(1):38-43. PubMed ID: 28413893
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  • 15. Evaluation of intervention strategy of thalassemia for couples of childbearing ages in Centre of Southern China.
    Jiang F, Zuo L, Li J, Chen G, Tang X, Zhou J, Qu Y, Li D, Liao C.
    J Clin Lab Anal; 2021 Oct; 35(10):e23990. PubMed ID: 34492731
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  • 19. Third-generation sequencing identified two rare α-chain variants leading to hemoglobin variants in Chinese population.
    Zhuang J, Jiang Y, Chen Y, Mao A, Chen J, Chen C.
    Mol Genet Genomic Med; 2024 Jan; 12(1):e2365. PubMed ID: 38284449
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