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Journal Abstract Search

90 related items for PubMed ID: 9050927

  • 21. Severity ranking of non-deletional alpha thalassemic alleles: insights from an Omani family study.
    Wali Y, Zadjali SA, Elshinawy M, Beshlawi I, Fawaz N, Alkindi S, Rawas A, Alsinani S, Daar S, Krishnamoorthy R.
    Eur J Haematol; 2011 Jun; 86(6):507-11. PubMed ID: 21410534
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  • 22. Introduction of novel α1-hemoglobin gene mutation with transfusion-dependent phenotype.
    Zekavat OR, Dehghani SJ, Imanifard J, Dehbozorgian J, Zareifar S, Haghpanah S.
    Hematology; 2017 Apr; 22(3):168-171. PubMed ID: 27665672
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  • 23. [Molecular detection and haematological analysis of heterozygotes in beta-thalassemia combining deletional alpha-thalassemia].
    Cai YL, Zheng YM, Tang MZ, Li J, Li SW.
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2007 Feb; 15(1):195-7. PubMed ID: 17490553
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  • 24. A novel α(0) -thalassemia deletion in a Greek patient with HbH disease and β-thalassemia trait.
    Phylipsen M, Traeger-Synodinos J, van der Kraan M, van Delft P, Bakker G, Geerts M, Kanavakis E, Stamoulakatou A, Karagiorga M, Giordano PC, Harteveld CL.
    Eur J Haematol; 2012 Apr; 88(4):356-62. PubMed ID: 22324317
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  • 25. Genotype-phenotype correlation and report of novel mutations in β-globin gene in thalassemia patients.
    Nagar R, Sinha S, Raman R.
    Blood Cells Mol Dis; 2015 Jun; 55(1):10-4. PubMed ID: 25976460
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  • 28. Complexity of the alpha-globin genotypes identified with thalassemia screening in Sardinia.
    Origa R, Paglietti ME, Sollaino MC, Desogus MF, Barella S, Loi D, Galanello R.
    Blood Cells Mol Dis; 2014 Jan; 52(1):46-9. PubMed ID: 23896219
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  • 31. An alpha0-thalassemia-like mutation: Hb Suan-Dok [alpha109(G16)Leu-->Arg] carried by a recombinant -alpha(3.7) gene.
    Moradkhani K, Mazurier E, Giordano PC, Wajcman H, Préhu C.
    Hemoglobin; 2008 Jan; 32(4):419-24. PubMed ID: 18654893
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  • 33. High frequency of deletional alpha-thalassemia in beta-thalassemia trait: implications for genetic counseling.
    Panigrahi I, Rafeeq PH, Choudhry VP, Saxena R.
    Am J Hematol; 2004 Jul; 76(3):297-9. PubMed ID: 15224373
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  • 34. [Molecular epidemiological analysis of α- and β-thalassemia in Fujian province].
    Xu LP, Huang HL, Wang Y, Zheng L, Wang LS, Xu JB, Huang XX, Lin Y.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Aug; 30(4):403-6. PubMed ID: 23926004
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  • 35. beta-Thalassemia in Sicily: hematological and biosynthetic studies.
    Schilirò G, Musumeci S, Pizzarelli G, Di Gregorio L, Fischer A, Russo G.
    Acta Haematol; 1978 Aug; 60(4):193-200. PubMed ID: 101006
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  • 36. Identification of Three Types of α-Thalassemia Deletion, -α21.9, -α2.4, and - -THAI, and Their Frequencies, in One Family in the Population of Southern Guangxi Zhuang Autonomous Region, People's Republic of China.
    Pang W, Long J, Weng X, Fan Q, Sun L, Pan Z, Fan Z.
    Hemoglobin; 2018 Jan; 42(1):37-42. PubMed ID: 29447013
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