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160 related items for PubMed ID: 6652684
21. Gamma delta beta-thalassemia due to a de novo mutation deleting the 5' beta-globin gene activation-region hypersensitive sites. Driscoll MC, Dobkin CS, Alter BP. Proc Natl Acad Sci U S A; 1989 Oct; 86(19):7470-4. PubMed ID: 2798417 [Abstract] [Full Text] [Related]
22. A novel deletion in delta beta-thalassemia found in Japan. Matsunaga E, Kimura A, Yamada H, Fukumaki Y, Takagi Y. Biochem Biophys Res Commun; 1985 Jan 16; 126(1):185-91. PubMed ID: 2982369 [Abstract] [Full Text] [Related]
23. The 3' ends of the deletions of Spanish delta beta zero-thalassemia and black HPFH 1 and 2 lie within 17 kilobases. Camaschella C, Serra A, Saglio G, Baiget M, Malgaretti N, Mantovani R, Ottolenghi S. Blood; 1987 Aug 16; 70(2):593-6. PubMed ID: 2440503 [Abstract] [Full Text] [Related]
24. Heterogeneity of DNA deletion in gamma delta beta-thalassemia. Orkin SH, Goff SC, Nathan DG. J Clin Invest; 1981 Mar 16; 67(3):878-84. PubMed ID: 6162860 [Abstract] [Full Text] [Related]
25. Changes in restricted human cellular DNA fragments containing globin gene sequences in thalassemias and related disorders. Mears JG, Ramirez F, Leibowitz D, Nakamura F, Bloom A, Konotey-Ahulu F, Bank A. Proc Natl Acad Sci U S A; 1978 Mar 16; 75(3):1222-6. PubMed ID: 274714 [Abstract] [Full Text] [Related]
27. Detection of germline rearrangements in patients with α- and β-thalassemia using high resolution array CGH. Blattner A, Brunner-Agten S, Ludin K, Hergersberg M, Herklotz R, Huber AR, Röthlisberger B. Blood Cells Mol Dis; 2013 Jun 16; 51(1):39-47. PubMed ID: 23491071 [Abstract] [Full Text] [Related]
29. Deletion of the A gamma-globin gene in G gamma-delta beta-thalassemia. Orkin SH, Alter BP, Altay C. J Clin Invest; 1979 Sep 16; 64(3):866-9. PubMed ID: 468997 [Abstract] [Full Text] [Related]
30. Partial deletion of beta-globin gene DNA in certain patients with beta 0-thalassemia. Orkin SH, Old JM, Weatherall DJ, Nathan DG. Proc Natl Acad Sci U S A; 1979 May 16; 76(5):2400-4. PubMed ID: 287080 [Abstract] [Full Text] [Related]
31. A distant gene deletion affects beta-globin gene function in an atypical gamma delta beta-thalassemia. Curtin P, Pirastu M, Kan YW, Gobert-Jones JA, Stephens AD, Lehmann H. J Clin Invest; 1985 Oct 16; 76(4):1554-8. PubMed ID: 2997283 [Abstract] [Full Text] [Related]
32. 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 Oct 16; 445():170-6. PubMed ID: 2409869 [No Abstract] [Full Text] [Related]
38. A deletion of the human beta-globin locus activation region causes a major alteration in chromatin structure and replication across the entire beta-globin locus. Forrester WC, Epner E, Driscoll MC, Enver T, Brice M, Papayannopoulou T, Groudine M. Genes Dev; 1990 Oct 15; 4(10):1637-49. PubMed ID: 2249769 [Abstract] [Full Text] [Related]
39. Phenotypic expression of Hb F in common high Hb F determinants in Thailand: roles of α-thalassemia, 5' δ-globin BCL11A binding region and 3' β-globin enhancer. Prakobkaew N, Fucharoen S, Fuchareon G, Siriratmanawong N. Eur J Haematol; 2014 Jan 15; 92(1):73-9. PubMed ID: 24112054 [Abstract] [Full Text] [Related]
40. A point mutation in the A gamma-globin gene promoter in Greek hereditary persistence of fetal haemoglobin. Collins FS, Metherall JE, Yamakawa M, Pan J, Weissman SM, Forget BG. Nature; 2014 Jan 15; 313(6000):325-6. PubMed ID: 2578620 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]