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659 related items for PubMed ID: 12827652
1. Spectrum of beta thalassemia mutations and HbF levels in the heterozygous Moroccan population. Lemsaddek W, Picanço I, Seuanes F, Mahmal L, Benchekroun S, Khattab M, Nogueira P, Osório-Almeida L. Am J Hematol; 2003 Jul; 73(3):161-8. PubMed ID: 12827652 [Abstract] [Full Text] [Related]
6. The clinical significance of the spectrum of interactions of CAP+1 (A-->C), a silent beta-globin gene mutation, with other beta-thalassemia mutations and globin gene modifiers in north Indians. Garewal G, Das R, Awasthi A, Ahluwalia J, Marwaha RK. Eur J Haematol; 2007 Nov; 79(5):417-21. PubMed ID: 17900295 [Abstract] [Full Text] [Related]
9. Asymptomatic and mild beta-thalassemia in homozygotes and compound heterozygotes for the IVS2+1G-->A mutation: role of the beta-globin gene haplotype. Ragusa A, Amata S, Lombardo T, Castiglia L, Maier-Redelsperger M, Labie D, Bernini L. Haematologica; 2003 Oct; 88(10):1099-105. PubMed ID: 14555304 [Abstract] [Full Text] [Related]
10. Spectrum of beta-thalassemia mutations and their association with allelic sequence polymorphisms at the beta-globin gene cluster in an Eastern Indian population. Kukreti R, Dash D, E VK, Chakravarty S, Das SK, De M, Talukder G. Am J Hematol; 2002 Aug; 70(4):269-77. PubMed ID: 12210807 [Abstract] [Full Text] [Related]
12. Screening of Iranian thalassemic families for the most common deletions of the beta-globin gene cluster. Esteghamat F, Imanian H, Azarkeivan A, Pourfarzad F, Almadani N, Najmabadi H. Hemoglobin; 2007 Aug; 31(4):463-9. PubMed ID: 17994380 [Abstract] [Full Text] [Related]
13. [Molecular-genetic characteristics of alpha, beta and delta beta-thalassemias in 139 heterozygotes in 56 unrelated Czech and Slovak families (Priority description of 3 beta-thalassemia mutations, an extensive alpha-thalassemia 2 (18+ kb) deletion and a Swiss-type nondeletion hereditary persistence of hemoglobin F)]. Indrák K, Divoký V, Brabec V, Indráková J, Svobodová M, Huisman TH. Vnitr Lek; 1993 Oct; 39(10):969-78. PubMed ID: 7694425 [Abstract] [Full Text] [Related]
16. [Beta-thalassemia mutations and single nucleotide polymorphism at -158 of Ggamma-globin gene associated with altered levels of Hb F in beta-thalassemia heterozygotes]. Chen JF, Long GF, Lin WX, Chen P. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Oct; 21(5):498-501. PubMed ID: 15476181 [Abstract] [Full Text] [Related]
19. Combined effect of two different polymorphic sequences within the beta globin gene cluster on the level of HbF. Gonçalves I, Ducrocq R, Lavinha J, Nogueira PJ, Peres MJ, Picanço I, Correia E, Reis AB, Silva C, Krishnamoorthy R, Almeida LO. Am J Hematol; 1998 Apr; 57(4):269-76. PubMed ID: 9544969 [Abstract] [Full Text] [Related]
20. Influence of Ggamma-158C --> and beta- (AT)x(T)y globin gene polymorphisms on HbF levels in Italian beta-thalassemia carriers and wild-type subjects. Guida V, Cappabianca MP, Colosimo A, Rafanelli F, Amato A, Dallapiccola B. Haematologica; 2006 Sep; 91(9):1275-6. PubMed ID: 16956833 [Abstract] [Full Text] [Related] Page: [Next] [New Search]