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Journal Abstract Search

227 related items for PubMed ID: 31703143

  • 1. [Clinical and genetic analysis of a patient with Hb Ottawa in conjunction with β -thalassemia].
    Ma X, Cai Z, Peng Y, Ma J, Zheng J, Cai G.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Nov 10; 36(11):1130-1132. PubMed ID: 31703143
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  • 3. [Analysis of clinical phenotype and genotype of unstable Hemoglobin Rush].
    Ge S, Yang B, Yi W, Huang K, Liu H, Huang X, Chu J, Yang Z.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Feb 10; 34(1):15-20. PubMed ID: 28186586
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  • 9. Analysis of rare thalassemia caused by HS-40 regulatory site deletion.
    Luo S, Chen X, Zhong Q, Wang Q, Xu Z, Qin L, Wang J, Yuan D, Yan T, Tang N.
    Hematology; 2020 Dec 10; 25(1):286-291. PubMed ID: 32720864
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  • 10. [Hematological Analysis and Diagnosis of Two Rare Abnormal Hemoglobin].
    Wang JC, Guo H, Huang HJ, Yuan TL, Yao CZ, Qin DQ, DU L.
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2020 Dec 10; 28(6):2028-2032. PubMed ID: 33283737
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  • 12. Five hemoglobin variants in a double heterozygote for α- and β-globin chain defects.
    Singha K, Fucharoen G, Fucharoen S.
    Acta Haematol; 2014 Dec 10; 131(2):71-5. PubMed ID: 24081021
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  • 13. Detection of Hb Constant Spring [α142, Term→Gln, TAA>CAA (α2)] in heterozygotes combined with β-thalassemia.
    Li YQ, Li R, Li DZ.
    Hemoglobin; 2013 Dec 10; 37(2):197-200. PubMed ID: 23390935
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  • 15. A novel (A)γδβ(0)-thalassemia caused by DNA deletion-inversion-insertion of the β-globin gene cluster and five olfactory receptor genes: Genetic interactions, hematological phenotypes and molecular characterization.
    Singha K, Fucharoen G, Hama A, Fucharoen S.
    Clin Biochem; 2015 Jul 10; 48(10-11):703-8. PubMed ID: 25866400
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