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22. The mutational basis of the thalassemia syndromes. Kazazian HH; Cho S; Phillips JA Prog Med Genet; 1977; 2():165-204. PubMed ID: 897199 [No Abstract] [Full Text] [Related]
23. Molecular pathology of alpha-thalassemia. Kan YW Ann N Y Acad Sci; 1985; 445():28-36. PubMed ID: 3860131 [TBL] [Abstract][Full Text] [Related]
24. The biochemical lesion in thalassaemia. Weatherall DJ Br J Haematol; 1968 Jul; 15(1):1-5. PubMed ID: 5660144 [No Abstract] [Full Text] [Related]
25. Deletion of alpha-globin genes in haemoglobin-H disease demonstrates multiple alpha-globin structural loci. Kan YW; Dozy AM; Varmus HE; Taylor JM; Holland JP; Lie-Injo LE; Ganesan J; Todd D Nature; 1975 May; 255(5505):255-6. PubMed ID: 1170497 [No Abstract] [Full Text] [Related]
26. Translation of -globin m-RNA in -thalassemia and the S and C hemoglobinopathies. Rieder RF J Clin Invest; 1972 Feb; 51(2):364-72. PubMed ID: 5009120 [TBL] [Abstract][Full Text] [Related]
28. Relative stability of alpha- and beta-globin messenger RNAs in homozygous beta+ thalassemia. Nienhuis AW; Turner P; Benz EJ Proc Natl Acad Sci U S A; 1977 Sep; 74(9):3960-4. PubMed ID: 71735 [TBL] [Abstract][Full Text] [Related]
29. Genetics of haemoglobin. Barkhan P Guys Hosp Rep; 1967; 116(3):307-22. PubMed ID: 4872865 [No Abstract] [Full Text] [Related]
30. Molecular genetics of human hemoglobin synthesis. Forget BG Ann Intern Med; 1979 Oct; 91(4):605-16. PubMed ID: 384860 [TBL] [Abstract][Full Text] [Related]
31. Heterogeneity of messenger RNA defects in the thalassemia syndromes. Benz EJ; Glass J; Tsistrakis GA; Hillman DG; Cavallesco C; Coupal E; Forget BG; Turner PA; Kantor JA; Nienhuis AW Ann N Y Acad Sci; 1980; 344():101-12. PubMed ID: 6930861 [No Abstract] [Full Text] [Related]
32. The molecular basis for abnormal gene action: recent lessons from the thalassaemia model. Weatherall DJ Clin Sci Mol Med; 1977 Mar; 52(3):223-7. PubMed ID: 66116 [No Abstract] [Full Text] [Related]
33. Regulation of hemoglobin synthesis in beta-thalassemia. Schwartz E; Gill FM Ann N Y Acad Sci; 1974; 232(0):33-9. PubMed ID: 4528708 [No Abstract] [Full Text] [Related]
34. [The hemoglobinopathies due to a disturbance of hemoglobin synthesis]. Labie D; Dreyfus JC Nouv Rev Fr Hematol; 1971; 11(1):83-93. PubMed ID: 4252108 [No Abstract] [Full Text] [Related]
35. [Molecular basis for differentiation of erythroid cells and regulation of the biosynthesis of individual types of hemoglobin]. Starodub NF Usp Sovrem Biol; 1980; 89(1):124-40. PubMed ID: 6994385 [No Abstract] [Full Text] [Related]
36. DNA and RNA defects in beta+ and beta 0 thalassemias. Bank A Tex Rep Biol Med; 1980-1981; 40():343-54. PubMed ID: 6172869 [No Abstract] [Full Text] [Related]
38. The severe form of alpha thalassaemia is caused by a haemoglobin gene deletion. Ottolenghi S; Lanyon WG; Paul J; Williamson R; Weatherall DJ; Clegg JB; Pritchard J; Pootrakul S; Boon WH Nature; 1974 Oct; 251(5474):389-92. PubMed ID: 4138824 [No Abstract] [Full Text] [Related]
39. The molecular defect of Ferrara beta-thalassemia. Conconi F; del Senno L Ann N Y Acad Sci; 1974; 232(0):54-64. PubMed ID: 4528795 [No Abstract] [Full Text] [Related]
40. Absence of messenger RNA for beta globin chain in beta(0) thalassaemia. Forget BG; Benz EJ; Skoultchi A; Baglioni C; Housman D Nature; 1974 Feb; 247(5440):379-81. PubMed ID: 4817859 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]