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Journal Abstract Search

179 related items for PubMed ID: 14747442

  • 21. Co-inheritance of Hb Pak Num Po, a novel alpha1 gene mutation, and alpha0 thalassemia associated with transfusion-dependent Hb H disease.
    Viprakasit V, Tanphaichitr VS, Veerakul G, Chinchang W, Petrarat S, Pung-Amritt P, Higgs DR.
    Am J Hematol; 2004 Mar; 75(3):157-63. PubMed ID: 14978697
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  • 23. 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; 48(10-11):703-8. PubMed ID: 25866400
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  • 24. A laboratory strategy for genotyping haemoglobin H disease in the Chinese.
    Chan AY, So CC, Ma ES, Chan LC.
    J Clin Pathol; 2007 Aug; 60(8):931-4. PubMed ID: 17018682
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  • 25. The molecular basis of alpha-thalassemia in Thailand.
    Winichagoon P, Fucharoen S, Wasi P.
    Southeast Asian J Trop Med Public Health; 1992 Aug; 23 Suppl 2():7-13. PubMed ID: 1298997
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  • 26. Characterization of two novel Alu element-mediated α-globin gene cluster deletions causing α0-thalassemia by targeted next-generation sequencing.
    Li Z, Shang X, Luo S, Zhu F, Wei X, Zhou W, Ye Y, Yan T, Cai R, Xu X.
    Mol Genet Genomics; 2020 Mar; 295(2):505-514. PubMed ID: 31897801
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  • 33. Development and validation of a zeta-globin-specific ELISA for carrier screening of the (--SEA) alpha thalassaemia deletion.
    Tang L, Zhu P, Zhou WJ, Zheng J, Zhou YQ, Fu N, Xu XM.
    J Clin Pathol; 2009 Feb; 62(2):147-51. PubMed ID: 19181632
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  • 35. The 32.6 kb Indian delta beta-thalassaemia deletion ends in a 3.4 kb L1 element downstream of the beta-globin gene.
    Gilman JG, Brinson EC, Mishima N.
    Br J Haematol; 1992 Oct; 82(2):417-21. PubMed ID: 1419824
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  • 36. Characterization of two unique α-globin gene cluster deletions causing α-thalassemia in Israeli Arabs.
    Gilad O, Dgany O, Noy-Lotan S, Krasnov T, Elitzur S, Pissard S, Kventsel I, Yacobovich J, Tamary H.
    Hemoglobin; 2014 Oct; 38(5):319-24. PubMed ID: 25222045
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  • 39. A new alpha-thalassemia-2 deletion resulting in microcytosis and hypochromia and in vitro chain imbalance in the heterozygote.
    Indrak K, Gu YC, Novotny J, Huisman TH.
    Am J Hematol; 1993 Jun; 43(2):144-5. PubMed ID: 8342542
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  • 40. Alpha-thalassaemia and globin gene rearrangements in French Polynesia.
    Philippon G, Martinson JJ, Rugless MJ, Moulia-Pelat JP, Plichart R, Roux JF, Martin PM, Clegg JB.
    Eur J Haematol; 1995 Sep; 55(3):171-7. PubMed ID: 7672089
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