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644 related items for PubMed ID: 18932074

  • 1.
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  • 2. alpha-thalassaemia masked by beta gene defects and a new polyadenylation site mutation on the alpha2-globin gene.
    Harteveld CL, Oosterhuis WP, Schoenmakers CH, Ananta H, Kos S, Bakker Verweij M, van Delft P, Arkesteijn SG, Phylipsen M, Giordano PC.
    Eur J Haematol; 2010 Apr; 84(4):354-8. PubMed ID: 19912309
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  • 3. Hb Sallanches [alpha104(G11)Cys-->Tyr, TGC>TAC] occurs frequently on the Indian subcontinent.
    Roy P, Bhattacharya G, Banerjee D, Chandra S, Ghosh M, Choudhuri U, Das M, Dasgupta UB.
    Hemoglobin; 2009 Apr; 33(6):486-91. PubMed ID: 19958194
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  • 4. Co-inheritance of the Hb Sun Prairie mutation with a point mutation at 5'-UTR in the eastern Indian population.
    Sarkar AA, Mukhopadhyay C, Chandra S, Banerjee S, Das MK, Dasgupta UB.
    Br J Haematol; 2005 Apr; 129(2):282-6. PubMed ID: 15813858
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  • 5. Thalassemias and other hemoglobinopathies in the Republic of Macedonia.
    Efremov GD.
    Hemoglobin; 2007 Apr; 31(1):1-15. PubMed ID: 17365000
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  • 6. Mutational spectrum of delta-globin gene in the Portuguese population.
    Morgado A, Picanço I, Gomes S, Miranda A, Coucelo M, Seuanes F, Seixas MT, Romão L, Faustino P.
    Eur J Haematol; 2007 Nov; 79(5):422-8. PubMed ID: 17916081
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  • 7. Extended molecular spectrum of beta- and alpha-thalassemia in Oman.
    Hassan SM, Hamza N, Jaffer Al-Lawatiya F, Jaffer Mohammed A, Harteveld CL, Rajab A, Giordano PC.
    Hemoglobin; 2010 Jan; 34(2):127-34. PubMed ID: 20353347
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  • 10. Hb Constant Spring [alpha 142, Term-->Gln (TAA>CAA in alpha2)] in the alpha-thalassemia of anemic patients in Myanmar.
    Ne-Win, Harano K, Harano T, Kyaw-Shwe, Aye-Aye-Myint, Khin-Thander-Aye, Okada S.
    Hemoglobin; 2008 Jan; 32(5):454-61. PubMed ID: 18932070
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  • 11. Spectrum of beta-globin gene mutations among thalassemia patients in the West Bank region of Palestine.
    Darwish HM, El-Khatib FF, Ayesh S.
    Hemoglobin; 2005 Jan; 29(2):119-32. PubMed ID: 15921164
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  • 12. Distinct phenotypic expression associated with a new hyperunstable alpha globin variant (Hb heraklion, alpha1cd37(C2)Pro>0): comparison to other alpha-thalassemic hemoglobinopathies.
    Traeger-Synodinos J, Papassotiriou I, Metaxotou-Mavrommati A, Vrettou C, Stamoulakatou A, Kanavakis E.
    Blood Cells Mol Dis; 2000 Aug; 26(4):276-84. PubMed ID: 11042028
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  • 13. Molecular epidemiological study of alpha- and beta-thalassemia in Sihui city.
    Tan JR, Li WJ, Ma JY, Mo QH, Li LY, Jia SQ, Lao XW, Li LY, He RQ, Xu XM.
    Di Yi Jun Yi Da Xue Xue Bao; 2003 Jul; 23(7):716-9. PubMed ID: 12865230
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  • 16. alpha-Thalassemia mutation analyses in Mazandaran province, North Iran.
    Tamaddoni A, Hadavi V, Nejad NH, Khosh-Ain A, Siami R, Aghai-Meibodi J, Almadani N, Oberkanins C, Law HY, Najmabadi H.
    Hemoglobin; 2009 Jul; 33(2):115-23. PubMed ID: 19373587
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  • 17. Hb Bleuland [alpha108(G15)Thr-->Asn, ACC-->AAC (alpha2)]: a new abnormal hemoglobin associated with a mild alpha-thalassemia phenotype.
    Harteveld CL, Versteegh FG, Kok PJ, van Rooijen-Nijdam IH, van Delft P, Giordano PC.
    Hemoglobin; 2006 Jul; 30(3):349-54. PubMed ID: 16840225
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  • 18. Multicenter study of the molecular basis of thalassemia intermedia in different ethnic populations.
    Verma IC, Kleanthous M, Saxena R, Fucharoen S, Winichagoon P, Raizuddin S, Khan SN, Akbari MT, Izadyar M, Kotea N, Old JM, Ioannou PA, Khan B.
    Hemoglobin; 2007 Jul; 31(4):439-52. PubMed ID: 17994378
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  • 19. The correlation of α-globin gene mutations and the XmnI polymorphism with clinical severity of Hb E/β-thalassemia.
    Charoenkwan P, Teerachaimahit P, Sanguansermsri T.
    Hemoglobin; 2014 Jul; 38(5):335-8. PubMed ID: 25238043
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  • 20. Variable presentation of HB H disease due to homozygosity for the rare polyadenylation signal A T(Indian) (AATAAA>AATA- -) mutation in four Indian families.
    Nair SB, Nadkarni AH, Ghosh K, Colah RB.
    Hemoglobin; 2013 Jul; 37(3):277-84. PubMed ID: 23517369
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