BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

185 related articles for article (PubMed ID: 1482661)

  • 1. Molecular characterization of a novel 10.3 kb deletion causing beta-thalassaemia with unusually high Hb A2.
    Craig JE; Kelly SJ; Barnetson R; Thein SL
    Br J Haematol; 1992 Dec; 82(4):735-44. PubMed ID: 1482661
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Australian beta zero-thalassaemia: a high haemoglobin A2 beta zero-thalassaemia due to a 12 kb deletion commencing 5' to the beta-globin gene.
    Motum PI; Lindeman R; Hamilton TJ; Trent RJ
    Br J Haematol; 1992 Sep; 82(1):107-13. PubMed ID: 1419783
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Filipino beta zero thalassaemia: a high Hb A2 beta zero thalassaemia resulting from a large deletion of the 5' beta globin gene region.
    Motum PI; Kearney A; Hamilton TJ; Trent RJ
    J Med Genet; 1993 Mar; 30(3):240-4. PubMed ID: 7682618
    [TBL] [Abstract][Full Text] [Related]  

  • 4. High hemoglobin A2 beta 0-thalassemia due to a 532-basepair deletion of the 5' beta-globin gene region.
    Waye JS; Cai SP; Eng B; Clark C; Adams JG; Chui DH; Steinberg MH
    Blood; 1991 Mar; 77(5):1100-3. PubMed ID: 1995096
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Molecular characterization of a high A2 beta thalassemia by direct sequencing of single strand enriched amplified genomic DNA.
    Thein SL; Hesketh C; Brown JM; Anstey AV; Weatherall DJ
    Blood; 1989 Mar; 73(4):924-30. PubMed ID: 2920214
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A genetic combination of silent beta-thalassaemia, high Hb A2 beta-thalassaemia, and single alpha globin gene deletion causing mild thalassaemia intermedia.
    Galanello R; Maccioni L; Rosatelli MC; Ibba P; Nurchi AM; Cao A
    J Med Genet; 1984 Apr; 21(2):153-6. PubMed ID: 6716419
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular characterization of a beta zero-thalassemia resulting from a 1.4 kilobase deletion.
    Anand R; Boehm CD; Kazazian HH; Vanin EF
    Blood; 1988 Aug; 72(2):636-41. PubMed ID: 2456798
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A beta zero-thalassaemia due to a 1605 bp deletion of the 5' beta-globin gene region.
    Dimovski AJ; Efremov DG; Jankovic L; Plaseska D; Juricic D; Efremov GD
    Br J Haematol; 1993 Sep; 85(1):143-7. PubMed ID: 8251381
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Interaction between deletion delta-thalassemia and beta zero-thalassemia (codon 39 nonsense mutation) in a Sardinian family.
    Galanello R; Podda A; Melis MA; Monne M; Cao A
    Prog Clin Biol Res; 1989; 316B():113-21. PubMed ID: 2482492
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Beta-thalassemia intermedia with exceptionally high hemoglobin A2: relationship to mutations in the beta-gene promoter.
    Coleman MB; Adams JG; Plonczynski MW; Harrell AH; Walker AM; Fairbanks V; Steinberg MH
    Am J Med Sci; 1992 Aug; 304(2):73-8. PubMed ID: 1380206
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Molecular characterization of a normal Hb A2 beta-thalassaemia determinant in a Sardinian family.
    Oggiano L; Pirastu M; Moi P; Longinotti M; Perseu L; Cao A
    Br J Haematol; 1987 Oct; 67(2):225-9. PubMed ID: 3676110
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A greater than 200 kb deletion removing the entire beta-like globin gene cluster in a family of Irish descent.
    Fortina P; Delgrosso K; Werner E; Haines K; Rappaport E; Schwartz E; Surrey S
    Hemoglobin; 1991; 15(1-2):23-41. PubMed ID: 1717405
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The 12.6 kilobase DNA deletion in Dutch beta zero-thalassaemia.
    Gilman JG
    Br J Haematol; 1987 Nov; 67(3):369-72. PubMed ID: 3689700
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The DNA deletion in an Indian delta beta-thalassaemia begins one kilobase from the A gamma globin gene and ends in an L1 repetitive sequence.
    Mishima N; Landman H; Huisman TH; Gilman JG
    Br J Haematol; 1989 Nov; 73(3):375-9. PubMed ID: 2605124
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A beta-thalassemia variant associated with unusually high hemoglobin A2 in an Iranian family.
    Thein SL; Barnetson R; Abdalla S
    Blood; 1992 May; 79(10):2801-3. PubMed ID: 1586730
    [No Abstract]   [Full Text] [Related]  

  • 16. Alpha zero- and beta zero-thalassemia in a Thai family: unusually mild homozygous beta zero-thalassemia without alpha-globin gene deletion.
    Yenchitsomanus P; Summers KM
    Hum Genet; 1985; 69(4):375-7. PubMed ID: 2580774
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A novel 105 basepair deletion causing beta(0)-thalassemia in members of a Thai family.
    Nopparatana C; Saechan V; Nopparatana C; Pornpatkul M; Panich V; Fukumaki Y
    Am J Hematol; 1999 May; 61(1):1-4. PubMed ID: 10331503
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Beta zero-thalassemia in a Thai family is caused by a 3.4 kb deletion including the entire beta-globin gene.
    Sanguansermsri T; Pape M; Laig M; Hundrieser J; Flatz G
    Hemoglobin; 1990; 14(2):157-68. PubMed ID: 2272839
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Hb S/beta zero-thalassemia due to the approximately 1.4-kb deletion is associated with a relatively mild phenotype.
    Waye JS; Chui DH; Eng B; Cai SP; Coleman MB; Adams JG; Steinberg MH
    Am J Hematol; 1991 Oct; 38(2):108-12. PubMed ID: 1719807
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The Corfu delta beta zero thalassemia: a small deletion acts at a distance to selectively abolish beta globin gene expression.
    Kulozik AE; Yarwood N; Jones RW
    Blood; 1988 Feb; 71(2):457-62. PubMed ID: 2827815
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.