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22. Study of hereditary persistence of fetal hemoglobin (P.H.F.Hb) in a sicilian family tree. Motta L; Polosa P Haematol Lat; 1966; 9(3):173-83. PubMed ID: 5989221 [No Abstract] [Full Text] [Related]
23. Molecular analysis of deletion and nondeletion hereditary persistence of fetal hemoglobin and identification of a new mutation causing beta-thalassemia. Feingold EA; Collins FS; Metherall JE; Stoeckert CJ; Weissman SM; Forget BG Ann N Y Acad Sci; 1985; 445():159-69. PubMed ID: 2409868 [No Abstract] [Full Text] [Related]
24. Heterogeneity of delta, beta-thalassemia and hereditary persistence of Hb F in the Mediterranean area. Ottolenghi S; Giglioni B; Comi P; Guida S; Casini C; Merli S; Mantovani R; Terragni F; Aghib D; Saglio G Ann N Y Acad Sci; 1985; 445():170-6. PubMed ID: 2409869 [No Abstract] [Full Text] [Related]
25. Changes in gene organization in the thalassemias. Mears JG; Ramirez F; Feldenzer J; Burns AL; Bank A Ann N Y Acad Sci; 1980; 344():41-7. PubMed ID: 6156629 [No Abstract] [Full Text] [Related]
26. Hereditary persistence of foetal haemoglobin in northwest India. Ghosh K; Hasan SW; Kumar S Trop Geogr Med; 1988 Jul; 40(3):209-12. PubMed ID: 2460980 [TBL] [Abstract][Full Text] [Related]
27. [Intermediate beta thalassemia of the delta-beta (0)/(delta-beta) (0) genotype. Report of a case]. Sáenz GF; Carrillo JM; Mora L; Chaves M; Rojas LG; Jiménez R; Jiménez J; Montero AG Sangre (Barc); 1984; 29(4-A):467-72. PubMed ID: 6209815 [No Abstract] [Full Text] [Related]
28. 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]
29. 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]
30. Nature of fetal hemoglobin in the Greek type of hereditary persistence of fetal hemoglobin with and without concurrent beta-thalassemia. Huisman TH; Schroeder WA; Stamatoyannopoulos G; Bouver N; Shelton JR; Shelton JB; Apell G J Clin Invest; 1970 May; 49(5):1035-40. PubMed ID: 5441539 [TBL] [Abstract][Full Text] [Related]
31. Molecular characterization of hereditary persistence of foetal haemoglobin mutation by restriction fragment length polymorphism mapping. Das SK; De M; Bhattacharya DK; Talukder G Cytobios; 2001; 106 Suppl 2():229-32. PubMed ID: 11545449 [TBL] [Abstract][Full Text] [Related]
32. Identification of novel candidate genes for globin regulation in erythroid cells containing large deletions of the human beta-globin gene cluster. de Andrade TG; Peterson KR; Cunha AF; Moreira LS; Fattori A; Saad ST; Costa FF Blood Cells Mol Dis; 2006; 37(2):82-90. PubMed ID: 16952470 [TBL] [Abstract][Full Text] [Related]
33. Molecular characterization of deletional forms of beta-thalassemia in Taiwan. Peng CT; Liu SC; Chiou SS; Kuo PL; Shih MC; Chang JY; Chang JG Ann Hematol; 2003 Jan; 82(1):33-6. PubMed ID: 12574962 [TBL] [Abstract][Full Text] [Related]
34. HbF production in adult life. Wood WG Prog Clin Biol Res; 1989; 316B():251-67. PubMed ID: 2482496 [No Abstract] [Full Text] [Related]
35. Genotypic heterogeneity and correlation to intergenic haplotype within high HbF beta-thalassemia intermedia. Papachatzopoulou A; Kourakli A; Makropoulou P; Kakagianne T; Sgourou A; Papadakis M; Athanassiadou A Eur J Haematol; 2006 Apr; 76(4):322-30. PubMed ID: 16519704 [TBL] [Abstract][Full Text] [Related]
36. Dissecting the loci controlling fetal haemoglobin production on chromosomes 11p and 6q by the regressive approach. Craig JE; Rochette J; Fisher CA; Weatherall DJ; Marc S; Lathrop GM; Demenais F; Thein S Nat Genet; 1996 Jan; 12(1):58-64. PubMed ID: 8528252 [TBL] [Abstract][Full Text] [Related]
37. 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; Rosatellí C; Galanello R; Villegas A Haematologica; 1999 Jan; 84(1):90-2. PubMed ID: 10091400 [No Abstract] [Full Text] [Related]
38. Simple fluorescent PCR method for detection of large deletions in the beta-globin gene cluster. De Andrade TG; Saad ST; Sonati Mde F; Costa FF Am J Hematol; 2003 Mar; 72(3):225-7. PubMed ID: 12605399 [TBL] [Abstract][Full Text] [Related]
39. The hereditary persistence of fetal hemoglobin syndromes: variations on the thalassemia theme. Kazazian HH Johns Hopkins Med J; 1976 Nov; 139(5):215-9. PubMed ID: 994361 [No Abstract] [Full Text] [Related]
40. [Changes in the hemoglobin fractions of nephroblastoma patients]. Sotnikova EN; Durnov LA; Zhordania RV; Gar'kavtseva RF; Bukhny AF Genetika; 1984 Feb; 20(2):357-61. PubMed ID: 6200383 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]