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Journal Abstract Search

806 related items for PubMed ID: 17365000

  • 21. Molecular and clinical features of Hb H disease in northern Thailand.
    Charoenkwan P, Taweephon R, Sae-Tung R, Thanarattanakorn P, Sanguansermsri T.
    Hemoglobin; 2005; 29(2):133-40. PubMed ID: 15921165
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  • 22. 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; 33(2):115-23. PubMed ID: 19373587
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  • 23. [Dominant beta-thalassemia alleles in the Czech and Slovak population (beta-thalassemia mutations in 112(T-A) and 121(G-T) codons and the unstable Hradec Králové hemoglobin or alpha 2 beta 2 115 (G17) Ala-Asp)].
    Indrák K, Divoký V, Brabec V, Chrobák L, Mociková K, Sakalová A, Svobodová M, Indráková J, Hammerová T, Zarnovicanová M.
    Vnitr Lek; 1994 Apr; 40(4):223-30. PubMed ID: 8184583
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  • 25. 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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  • 32. 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 Aug; 31(4):439-52. PubMed ID: 17994378
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  • 33. Molecular spectrum of α- and β-globin gene mutations detected in the population of Guangxi Zhuang Autonomous Region, People's Republic of China.
    Zheng CG, Liu M, Du J, Chen K, Yang Y, Yang Z.
    Hemoglobin; 2011 Aug; 35(1):28-39. PubMed ID: 21250879
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  • 34. [Molecular characterization of thalassemias in the Valencia community and its relationship with the hematological phenotype].
    Pérez Sirvent M, Moreno Miralles I, Boluferx Gilabert P, Lerma Alejos E, Gómez Rejas MA, Vayá Montaña A, Tascón Astigarraga A, Dasí Carpio MA, Martínez Silvestre M, López Espinosa AR, Hernández Mateo L, Gil Alfonso R.
    Sangre (Barc); 1998 Oct; 43(5):392-8. PubMed ID: 9868331
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  • 35. Molecular spectrum of β-thalassemia mutations in the admixed Venezuelan population, and their linkage to β-globin gene haplotypes.
    Bravo-Urquiola M, Arends A, Gómez G, Montilla S, Gerard N, Chacin M, Berbar T, García O, García G, Velasquez D, Castillo O, Krishnamoorthy R.
    Hemoglobin; 2012 Oct; 36(3):209-18. PubMed ID: 22563936
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  • 38. Molecular lesion frequency of hemoglobin gene disorders in Taiwan.
    Liu SC, Peng CT, Lin TH, Wang SJ, Shih MC, Tien N, Chang CC, Lu JJ, Lin CY.
    Hemoglobin; 2011 Oct; 35(3):228-36. PubMed ID: 21599435
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  • 39. Molecular characterization and phenotypical study of β-thalassemia in Tucumán, Argentina.
    Lazarte SS, Mónaco ME, Haro AC, Jiménez CL, Ledesma Achem ME, Issé BA.
    Hemoglobin; 2014 Oct; 38(6):394-401. PubMed ID: 25347257
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  • 40. Molecular epidemiological survey of hemoglobinopathies in the Wuxi region of Jiangsu Province, eastern China.
    Lin M, Han ZJ, Wang Q, Zheng L, Wang Y, Yang H, Huang Y, Lin F, Zhan XF, Lin CP, Wu JR, Luo ZY, Liu JB, Yan ZH, Zheng SY, Zheng JK, Lu M, Zhu JJ, Xie LX, Yang LY.
    Hemoglobin; 2013 Oct; 37(5):454-66. PubMed ID: 23806067
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