These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

165 related articles for article (PubMed ID: 1550780)

  • 1. Promoter mutations producing mild beta-thalassaemia in the Italian population.
    Meloni A; Rosatelli MC; FaĆ  V; Sardu R; Saba L; Murru S; Sciarratta GV; Baldi M; Tannoia N; Vitucci A
    Br J Haematol; 1992 Feb; 80(2):222-6. PubMed ID: 1550780
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The C-T substitution in the distal CACCC box of the beta-globin gene promoter is a common cause of silent beta thalassaemia in the Italian population.
    Ristaldi MS; Murru S; Loudianos G; Casula L; Porcu S; Pigheddu D; Fanni B; Sciarratta GV; Agosti S; Parodi MI
    Br J Haematol; 1990 Apr; 74(4):480-6. PubMed ID: 2346726
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A beta-thalassaemia phenotype not linked to the beta-globin cluster in an Italian family.
    Murru S; Loudianos G; Porcu S; Sciarratta GV; Agosti S; Parodi MI; Cao A; Pirastu M
    Br J Haematol; 1992 Jun; 81(2):283-7. PubMed ID: 1643026
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Molecular characterization of beta-thalassemia intermedia in patients of Italian descent and identification of three novel beta-thalassemia mutations.
    Murru S; Loudianos G; Deiana M; Camaschella C; Sciarratta GV; Agosti S; Parodi MI; Cerruti P; Cao A; Pirastu M
    Blood; 1991 Mar; 77(6):1342-7. PubMed ID: 2001456
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Molecular characterization of beta-globin gene mutations in patients with beta-thalassaemia intermedia in south China.
    Antonarakis SE; Kang J; Lam VM; Tam JW; Li AM
    Br J Haematol; 1988 Nov; 70(3):357-61. PubMed ID: 3207629
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Molecular, haematological and clinical studies of the -101 C --> T substitution of the beta-globin gene promoter in 25 beta-thalassaemia intermedia patients and 45 heterozygotes.
    Maragoudaki E; Kanavakis E; Traeger-Synodinos J; Vrettou C; Tzetis M; Metaxotou-Mavrommati A; Kattamis C
    Br J Haematol; 1999 Dec; 107(4):699-706. PubMed ID: 10606872
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Rare beta-thalassaemia mutations in Asian indians.
    Varawalla NY; Old JM; Weatherall DJ
    Br J Haematol; 1991 Dec; 79(4):640-4. PubMed ID: 1772786
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Molecular, haematological and clinical studies of a silent beta-gene C-->G mutation at 6 bp 3' to the termination codon (+1480 C-->G) in twelve Greek families.
    Maragoudaki E; Vrettou C; Kanavakis E; Traeger-Synodinos J; Metaxotou-Mavrommati A; Kattamis C
    Br J Haematol; 1998 Oct; 103(1):45-51. PubMed ID: 9792288
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Beta thalassemia in Germany: molecular genetics and clinical phenotype in immigrant and in the native population].
    Schwarz C; Vetter B; Kohne E; Kulozik AE
    Klin Padiatr; 1997; 209(4):172-7. PubMed ID: 9340427
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Homozygous beta-thalassaemia resulting in the beta-thalassaemia carrier state phenotype.
    Rosatelli MC; Pischedda A; Meloni A; Saba L; Pomo A; Travi M; Fattore S; Cao A
    Br J Haematol; 1994 Nov; 88(3):562-5. PubMed ID: 7819068
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Severe thalassaemia intermedia caused by interaction of homozygosity for alpha-globin gene triplication with heterozygosity for beta zero-thalassaemia.
    Oron V; Filon D; Oppenheim A; Rund D
    Br J Haematol; 1994 Feb; 86(2):377-9. PubMed ID: 8199028
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A benign form of thalassaemia intermedia may be determined by the interaction of triplicated alpha locus and heterozygous beta-thalassaemia.
    Camaschella C; Bertero MT; Serra A; Dall'Acqua M; Gasparini P; Trento M; Vettore L; Perona G; Saglio G; Mazza U
    Br J Haematol; 1987 May; 66(1):103-7. PubMed ID: 3593644
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular heterogeneity of beta-thalassaemia in the Japanese: identification of two novel mutations.
    Fucharoen S; Katsube T; Fucharoen G; Sawada H; Oishi H; Katsuno M; Nishimura J; Motomura S; Miura Y; Fukumaki Y
    Br J Haematol; 1990 Jan; 74(1):101-7. PubMed ID: 2310691
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Homozygous beta+ thalassaemia owing to a mutation in the cleavage-polyadenylation sequence of the human beta globin gene.
    Losekoot M; Fodde R; Harteveld CL; van Heeren H; Giordano PC; Went LN; Bernini LF
    J Med Genet; 1991 Apr; 28(4):252-5. PubMed ID: 1856830
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Molecular basis and haematological characterization of beta-thalassaemia major in Taiwan, with a mutation of IVS-1 3' end TAG-->GAG in a Chinese patient.
    Chiou SS; Chang TT; Chen PH; Lee LS; Chen TS; Chang JG
    Br J Haematol; 1993 Jan; 83(1):112-7. PubMed ID: 8435318
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Molecular characterization of beta-globin gene mutations in Malay patients with Hb E-beta-thalassaemia and thalassaemia major.
    Yang KG; Kutlar F; George E; Wilson JB; Kutlar A; Stoming TA; Gonzalez-Redondo JM; Huisman TH
    Br J Haematol; 1989 May; 72(1):73-80. PubMed ID: 2736244
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Spontaneous mutation in beta-thalassaemia producing the same nucleotide substitution as that in a common hereditary form.
    Chehab FF; Honig GR; Kan YW
    Lancet; 1986 Jan; 1(8471):3-5. PubMed ID: 2867271
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Delta-thalassemia due to a mutation in an erythroid-specific binding protein sequence 3' to the delta-globin gene.
    Moi P; Loudianos G; Lavinha J; Murru S; Cossu P; Casu R; Oggiano L; Longinotti M; Cao A; Pirastu M
    Blood; 1992 Jan; 79(2):512-6. PubMed ID: 1309671
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. A novel beta-delta globin gene fusion, anti-Lepore Hong Kong, leads to overexpression of delta globin chain and a mild thalassaemia intermedia phenotype when co-inherited with beta(0)-thalassaemia.
    So CC; Chan AY; Tsang ST; Lee AC; Au WY; Ma ES; Chan LC
    Br J Haematol; 2007 Jan; 136(1):158-62. PubMed ID: 17222202
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.