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4. Compound heterozygosity of non-deletional hereditary persistence of fetal hemoglobin and deltabeta-thalassemia. Kalamaras A; Chassanidis C; Samara M; Papadakis MN; Vagena A; Aleporou-Marinou V; Patrinos GP; Kollia P Am J Hematol; 2008 Sep; 83(9):760. PubMed ID: 18615450 [No Abstract] [Full Text] [Related]
5. Allele-specific transcription of fetal genes in primary erythroid cell cultures from Lepore and deltabeta degrees thalassemia patients. Di Marzo R; Acuto S; Calzolari R; Maggio A Exp Hematol; 2005 Nov; 33(11):1363-70. PubMed ID: 16263421 [TBL] [Abstract][Full Text] [Related]
6. Disorders of the synthesis of human fetal hemoglobin. Manca L; Masala B IUBMB Life; 2008 Feb; 60(2):94-111. PubMed ID: 18379999 [TBL] [Abstract][Full Text] [Related]
7. C-->T mutation at -158 G gamma HPFH associated with 4 bp deletion (-225-222) in the promoter region of the A gamma gene in homozygous beta 0 39 nonsense thalassemia. Ataulfo Gonzalez F; Ropero P; Sánchez J; Rosatellà C; Galanello R; Villegas A Haematologica; 1999 Jan; 84(1):90-2. PubMed ID: 10091400 [No Abstract] [Full Text] [Related]
8. Promoter choice within a gene cluster: a switch of loyalties. Whitelaw E Bioessays; 1990 Jun; 12(6):283-5. PubMed ID: 1696814 [No Abstract] [Full Text] [Related]
9. The emerging complexity of genetic control of persistent fetal hemoglobin biosynthesis in adults. Boyer SH Ann N Y Acad Sci; 1989; 565():23-36. PubMed ID: 2476063 [No Abstract] [Full Text] [Related]
11. Concordant fetal hemoglobin response to hydroxyurea in siblings with sickle cell disease. Steinberg MH; Voskaridou E; Kutlar A; Loukopoulos D; Koshy M; Ballas SK; Castro O; Barton F Am J Hematol; 2003 Feb; 72(2):121-6. PubMed ID: 12555216 [TBL] [Abstract][Full Text] [Related]
12. G gamma-196 C-->T, A gamma-201 C-->T: two novel mutations in the promoter region of the gamma-globin genes associated with nondeletional hereditary persistence of fetal hemoglobin in Greece. Tasiopoulou M; Boussiou M; Sinopoulou K; Moraitis G; Loutradi-Anagnostou A; Karababa P Blood Cells Mol Dis; 2008; 40(3):320-2. PubMed ID: 18096417 [TBL] [Abstract][Full Text] [Related]
13. 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 [TBL] [Abstract][Full Text] [Related]
14. Modulation of fetal hemoglobin synthesis by iron deficiency. Adams JG; Coleman MB; Hayes J; Morrison WT; Steinberg MH N Engl J Med; 1985 Nov; 313(22):1402-5. PubMed ID: 2414661 [No Abstract] [Full Text] [Related]
15. Molecular studies of mutations that increase Hb F production in man. Forget BG; Tuan D; Newman MV; Feingold EA; Collins F; Fukumaki Y; Jagadeeswaran P; Weissman SM Prog Clin Biol Res; 1983; 134():65-76. PubMed ID: 6198666 [No Abstract] [Full Text] [Related]
16. Ggamma -37 (A-->T): a new nondeletional hereditary persistence of fetal hemoglobin determinant associated with the rare codon 91 (+T) delta0-thalassemia. Bouva MJ; Harteveld CL; Bakker-Verweij G; van Delft P; Giordano PC Hemoglobin; 2006; 30(3):371-7. PubMed ID: 16840228 [TBL] [Abstract][Full Text] [Related]
17. Genetic and molecular analysis of mild forms of homozygous beta-thalassemia. Weatherall DJ; Wainscoat JS; Thein SL; Old JM; Wood WG; Higgs DR; Clegg JB Ann N Y Acad Sci; 1985; 445():68-80. PubMed ID: 2409878 [No Abstract] [Full Text] [Related]
18. Gene deletion in hereditary persistence of fetal hemoglobin (HPFH) and delta beta thalassemia. Mears JG Tex Rep Biol Med; 1980-1981; 40():365-72. PubMed ID: 6172870 [No Abstract] [Full Text] [Related]
19. A novel frameshift mutation (+A) at codon 18 of the beta-globin gene associated with high persistence of fetal hemoglobin phenotype and deltabeta-thalassemia. Feriotto G; Salvatori F; Finotti A; Breveglieri G; Venturi M; Zuccato C; Bianchi N; Borgatti M; Lampronti I; Mancini I; Massei F; Favre C; Gambari R Acta Haematol; 2008; 119(1):28-37. PubMed ID: 18230963 [TBL] [Abstract][Full Text] [Related]
20. 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 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]