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Journal Abstract Search

77 related items for PubMed ID: 3689948

  • 1. Multiple origins of the beta-thalassemia gene with a four-nucleotide deletion in its second exon.
    Fukumaki Y, Matsunaga E, Takihara Y, Nakamura T, Takagi Y, Tanphaichitr VS, Suvatte V, Tuchinda S, Lin ST, Lee HT.
    Birth Defects Orig Artic Ser; 1987; 23(5A):81-5. PubMed ID: 3689948
    [No Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. Quantification analysis of splice signal sequences. Exon skipping in beta-globin gene of thalassemia.
    Iida Y.
    Nucleic Acids Symp Ser; 1993; (29):161-2. PubMed ID: 8247751
    [Abstract] [Full Text] [Related]

  • 4. Beta-thalassemia in Chinese--analysis of polymorphic restriction site haplotypes in the beta-globin gene cluster.
    Huang SZ, Kazazian HH, Waber PG, Luo HY, Cai RL, Wang MQ.
    Chin Med J (Engl); 1985 Dec; 98(12):881-6. PubMed ID: 3009101
    [No Abstract] [Full Text] [Related]

  • 5. "Silent" nucleotide substitution in codon 24 of a beta+ thalassemia globin gene activates splice site in coding sequence RNA.
    Humphries RK, Ley T, Goldsmith ME, Kantor JA, Cline AC, Nienhuis AW.
    Prog Clin Biol Res; 1983 Dec; 134():123-6. PubMed ID: 6664994
    [Abstract] [Full Text] [Related]

  • 6. Polymorphism and molecular pathology of the human beta-globin gene.
    Orkin SH, Antonarakis SE, Kazazian HH.
    Prog Hematol; 1983 Dec; 13():49-73. PubMed ID: 6366914
    [No Abstract] [Full Text] [Related]

  • 7. Three-base deletion in exon 3 of the beta-globin gene produced a novel variant (beta gunma) with a thalassemia-like phenotype.
    Fucharoen S, Fucharoen G, Fukumaki Y, Nakayama Y, Hattori Y, Yamamoto K, Ohba Y.
    Blood; 1990 Nov 01; 76(9):1894-6. PubMed ID: 2224139
    [No Abstract] [Full Text] [Related]

  • 8. Dominantly Inherited beta-Thalassemia.
    Efremov GD.
    Hemoglobin; 2007 Nov 01; 31(2):193-207. PubMed ID: 17486503
    [Abstract] [Full Text] [Related]

  • 9. Beta-globin gene disorders in Italy and the Mediterranean area.
    Ottolenghi S, Carestia C.
    Horiz Biochem Biophys; 1986 Nov 01; 8():257-98. PubMed ID: 2875932
    [No Abstract] [Full Text] [Related]

  • 10. Dominant thalassemia-like phenotypes associated with mutations in exon 3 of the beta-globin gene.
    Kazazian HH, Dowling CE, Hurwitz RL, Coleman M, Stopeck A, Adams JG.
    Blood; 1992 Jun 01; 79(11):3014-8. PubMed ID: 1586746
    [Abstract] [Full Text] [Related]

  • 11. A new codon 31 (-C) mutant resulting in beta zero-thalassemia.
    Lin LI, Lin KS, Lin KH.
    Proc Natl Sci Counc Repub China B; 1992 Jan 01; 16(1):6-9. PubMed ID: 1631246
    [Abstract] [Full Text] [Related]

  • 12. alpha-globin gene deletions associated with Hb J Tongariki.
    Bowden DK, Pressley L, Higgs DR, Clegg JB, Weatherall DJ.
    Br J Haematol; 1982 Jun 01; 51(2):243-9. PubMed ID: 6979350
    [Abstract] [Full Text] [Related]

  • 13. The novo 4 BP deletion in the codons 20/21 (-TGGA) at the first exon of the beta-globin gene causing a beta0-thalassemia in a Spanish male.
    Ropero P, González FA, Villas JM, Paúl R, Villegas A.
    Ann Hematol; 2008 Jan 01; 87(1):63-5. PubMed ID: 17661037
    [No Abstract] [Full Text] [Related]

  • 14. Use of haplotype analysis in the beta-globin gene cluster to discover beta-thalassemia mutations.
    Kazazian HH, Antonarakis SE, Cheng T, Boehm CD, Waber PG.
    Prog Clin Biol Res; 1983 Jan 01; 134():91-8. PubMed ID: 6665005
    [Abstract] [Full Text] [Related]

  • 15. Linkage between fetal A gamma globin chain polymorphism and DNA polymorphism of the human beta gene cluster in beta thalassaemia.
    Beldjord C, Arbane M, Lapoumeroulie C, Rouyer-Fessard P, Benabadji M, Labie D, Beuzard Y.
    Mol Biol Med; 1984 Aug 01; 2(4):301-6. PubMed ID: 6100562
    [Abstract] [Full Text] [Related]

  • 16. beta-Thalassemia due to a deletion of the nucleotide which is substituted in the beta S-globin gene.
    Kazazian HH, Orkin SH, Boehm CD, Sexton JP, Antonarakis SE.
    Am J Hum Genet; 1983 Sep 01; 35(5):1028-33. PubMed ID: 6310991
    [Abstract] [Full Text] [Related]

  • 17. Globin gene mapping studies in Sardinian patients homozygous for beta zero Thalassaemia.
    Wainscoat JS, Bell JI, Old JM, Weatherall DJ, Furbetta M, Galanello R, Cao A.
    Mol Biol Med; 1983 Jul 01; 1(1):1-10. PubMed ID: 6092822
    [Abstract] [Full Text] [Related]

  • 18. Eight-base deletion in exon 3 of the beta-globin gene produced a novel variant (beta khon kaen) with an inclusion body beta-thalassemia trait.
    Fucharoen G, Fuchareon S, Jetsrisuparb A, Fukumaki Y.
    Blood; 1991 Jul 15; 78(2):537-9. PubMed ID: 2070092
    [No Abstract] [Full Text] [Related]

  • 19. DNA analysis as clinical investigation: when and how?
    Jeanpierre M, Junien C.
    Ann Genet; 1984 Jul 15; 27(3):134-47. PubMed ID: 6095729
    [No Abstract] [Full Text] [Related]

  • 20. 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 15; 70(4):269-77. PubMed ID: 12210807
    [Abstract] [Full Text] [Related]

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