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Journal Abstract Search

150 related items for PubMed ID: 33283737

  • 1. [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; 28(6):2028-2032. PubMed ID: 33283737
    [Abstract] [Full Text] [Related]

  • 2. Compound heterozygosity for hemoglobin variant Hb-Broomhill and the Southeast Asian α-thalassemia deletion does not worsen outcome: a case report of two unrelated patients.
    Qin D, Du L, Wang J, Yao C, Guo H, Yuan T, Liang J, Yin A.
    J Int Med Res; 2020 Nov; 48(11):300060520967825. PubMed ID: 33213249
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  • 5. Association of Hb Thailand [α56(E5)Lys→Thr] and Hb Phnom Penh [α117(GH5)-Ile-α118(H1)] with α(0)-thalassemia: molecular and hematological features and differential diagnosis.
    Singha K, Srivorakun H, Fucharoen G, Changtrakul Y, Komwilaisak P, Jetsrisuparb A, Puangplruk R, Fucharoen S.
    Hemoglobin; 2013 Nov; 37(1):37-47. PubMed ID: 23215800
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  • 7. Comparison of capillary electrophoregram among heterozygous Hb Hope, Hb Hope/α-thalassemia-1 SEA type deletion and Hb Hope/β(0)-thalassemia.
    Pornprasert S, Panyasai S, Kongthai K.
    Clin Chem Lab Med; 2012 Mar 07; 50(9):1625-9. PubMed ID: 22962223
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  • 8. [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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  • 9. Uncommon Combination of Hemoglobin Jax and Hemoglobin Constant Spring Leading to Microcytic Anemia.
    Srichairatanakool S, Chai-Adisaksopha C, Tantiworawit A, Phusua A, Charoenkwan P.
    Am J Case Rep; 2024 May 10; 25():e943560. PubMed ID: 38725231
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  • 10. [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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  • 12. [A study on gene mutation spectrums of α- and β-thalassemias in populations of Yunnan Province and the prenatal gene diagnosis].
    Zhu BS, He J, Zhang J, Zeng XH, Su J, Xu XH, Li SY, Chen H, Zhang YH.
    Zhonghua Fu Chan Ke Za Zhi; 2012 Feb 10; 47(2):85-9. PubMed ID: 22455737
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  • 13. Analysis of fetal blood using capillary electrophoresis system: a simple method for prenatal diagnosis of severe thalassemia diseases.
    Srivorakun H, Fucharoen G, Sae-Ung N, Sanchaisuriya K, Ratanasiri T, Fucharoen S.
    Eur J Haematol; 2009 Jul 10; 83(1):57-65. PubMed ID: 19226360
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  • 15. Hematological and molecular characteristics of a novel α-globin variant Hb Liangqing (HBA2:c.224A>G).
    Li Y, Liang S, Liang L, Zheng L, Lu X.
    Hematology; 2023 Dec 10; 28(1):2213545. PubMed ID: 37213176
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  • 16. Hb Knossos (HBB: c.82G > T), β-globin CD 5 (-CT) (HBB: c.17_18delCT) and δ-globin CD 59 (-a) (HBD: c.179delA) mutations in a Syrian patient with β-thalassemia intermedia.
    Moassas F, Nweder MS, Murad H.
    BMC Pediatr; 2019 Feb 18; 19(1):61. PubMed ID: 30777047
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  • 17. Complex interaction of Hb E [beta26(B8)Glu-->Lys], Hb Korle-Bu [beta73(E17)Asp-->Asn] and a deletional alpha-thalassemia-1 in pregnancy.
    Siriratmanawong N, Chansri W, Singsanan S, Fucharoen G, Fucharoen S.
    Hemoglobin; 2009 Feb 18; 33(6):507-14. PubMed ID: 19958198
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  • 19. [Diagnosis and prenatal diagnosis to a family of hemoglobin variant with α-thalassemia].
    Du L, Wu J, Qin D, Wang J, Luo M, Guo H, Yuan T, Zhang Y, Wang Y, Yin A.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Apr 18; 32(2):226-8. PubMed ID: 25863092
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  • 20. Microcytic hypochromic anemia patients with thalassemia: genotyping approach.
    Rahim F.
    Indian J Med Sci; 2009 Mar 18; 63(3):101-8. PubMed ID: 19359777
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