457 related articles for article (PubMed ID: 15566365)
1. Somatic deletion of the normal beta-globin gene leading to thalassaemia intermedia in heterozygous beta-thalassaemic patients.
Galanello R; Perseu L; Perra C; Maccioni L; Barella S; Longinotti M; Cao A; Cazzola M
Br J Haematol; 2004 Dec; 127(5):604-6. PubMed ID: 15566365
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. High frequency of deletional alpha-thalassemia in beta-thalassemia trait: implications for genetic counseling.
Panigrahi I; Rafeeq PH; Choudhry VP; Saxena R
Am J Hematol; 2004 Jul; 76(3):297-9. PubMed ID: 15224373
[TBL] [Abstract][Full Text] [Related]
5. Mutational spectrum of delta-globin gene in the Portuguese population.
Morgado A; Picanço I; Gomes S; Miranda A; Coucelo M; Seuanes F; Seixas MT; Romão L; Faustino P
Eur J Haematol; 2007 Nov; 79(5):422-8. PubMed ID: 17916081
[TBL] [Abstract][Full Text] [Related]
6. Globin chain synthesis analysis in obligate beta 0-thalassemia heterozygotes with isolated increase of hemoglobin A2 levels.
Galanello R; Melis MA; Furbetta M; Angius A; Scalas MT; Paglietti E; Cao A
Nouv Rev Fr Hematol (1978); 1981; 23(4):193-5. PubMed ID: 7312613
[TBL] [Abstract][Full Text] [Related]
7. A novel frameshift mutation (+G) at codons 15/16 in a beta0 thalassaemia gene results in a significant reduction of beta globin mRNA values.
Mo QH; Li XR; Li CF; He YL; Xu XM
J Clin Pathol; 2005 Sep; 58(9):923-6. PubMed ID: 16126871
[TBL] [Abstract][Full Text] [Related]
8. Segmental duplications involving the alpha-globin gene cluster are causing beta-thalassemia intermedia phenotypes in beta-thalassemia heterozygous patients.
Harteveld CL; Refaldi C; Cassinerio E; Cappellini MD; Giordano PC
Blood Cells Mol Dis; 2008; 40(3):312-6. PubMed ID: 18249014
[TBL] [Abstract][Full Text] [Related]
9. Frequency of delta+ 27-thalassaemia in Sardinians.
Guiso L; Frogheri L; Pistidda P; Angioni L; Dore F; Pardini S; Longinotti M
Clin Lab Haematol; 1996 Dec; 18(4):241-4. PubMed ID: 9054695
[TBL] [Abstract][Full Text] [Related]
10. Heterogeneity of beta/alpha ratio in Italian beta-thalassaemia heterozygotes.
Sampietro M; Cappellini MD; Taddei MT; Fiorelli G
Haematologica; 1983; 68(6):703-11. PubMed ID: 6199264
[No Abstract] [Full Text] [Related]
11. Thalassaemia-like carriers not linked to the beta-globin gene cluster.
Faà V; Meloni A; Moi L; Ibba G; Travi M; Vitucci A; Cao A; Rosatelli MC
Br J Haematol; 2006 Mar; 132(5):640-50. PubMed ID: 16445840
[TBL] [Abstract][Full Text] [Related]
12. [Thalassemia intermedia caused by interaction of IVS-1 1(G--A) mutation in the beta-globin gene and heterozygotic triplication in the alpha-globin gene].
Martínez-López J; Galán García P; del Río E; Baiget M; Gilsanz Rodríguez F
Rev Clin Esp; 1998 Mar; 198(3):153-5. PubMed ID: 9586437
[TBL] [Abstract][Full Text] [Related]
13. 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
[TBL] [Abstract][Full Text] [Related]
14. Co-inheritance of compound heterozygous Hb Constant Spring and a single -alpha(3.7) gene deletion with heterozygous deltabeta thalassaemia: a diagnostic challenge.
Azma RZ; Othman A; Azman N; Alauddin H; Ithnin A; Yusof N; Razak NF; Sardi NH; Hussin NH
Malays J Pathol; 2012 Jun; 34(1):57-62. PubMed ID: 22870600
[TBL] [Abstract][Full Text] [Related]
15. A novel mutation of -73(A-->T) in the CCAAT box of the beta-globin gene identified in a patient with the mild beta-thalassemia intermedia.
Chen XW; Mo QH; Li Q; Zeng R; Xu XM
Ann Hematol; 2007 Sep; 86(9):653-7. PubMed ID: 17516066
[TBL] [Abstract][Full Text] [Related]
16. Haematological phenotypes in a family with triplicated alpha-globin gene, beta zero 39 and delta+27 thalassaemia mutations.
Oggiano L; Rimini E; Frogheri L; Guiso L; Pistidda P; Longinotti M
Clin Lab Haematol; 1992; 14(4):289-92. PubMed ID: 1478008
[TBL] [Abstract][Full Text] [Related]
17. Beta-thalassemia intermedia due to compound heterozygosity for two beta-globin gene promoter mutations, including a novel TATA box deletion.
Basran RK; Reiss UM; Luo HY; Ware RE; Chui DH
Pediatr Blood Cancer; 2008 Feb; 50(2):363-6. PubMed ID: 16732578
[TBL] [Abstract][Full Text] [Related]
18. Genotypic heterogeneity and correlation to intergenic haplotype within high HbF beta-thalassemia intermedia.
Papachatzopoulou A; Kourakli A; Makropoulou P; Kakagianne T; Sgourou A; Papadakis M; Athanassiadou A
Eur J Haematol; 2006 Apr; 76(4):322-30. PubMed ID: 16519704
[TBL] [Abstract][Full Text] [Related]
19. Allele-specific transcription of fetal genes in primary erythroid cell cultures from Lepore and deltabeta degrees thalassemia patients.
Di Marzo R; Acuto S; Calzolari R; Maggio A
Exp Hematol; 2005 Nov; 33(11):1363-70. PubMed ID: 16263421
[TBL] [Abstract][Full Text] [Related]
20. Molecular basis and hematologic characterization of deltabeta-thalassemia and hereditary persistence of fetal hemoglobin in Thailand.
Panyasai S; Fucharoen S; Surapot S; Fucharoen G; Sanchaisuriya K
Haematologica; 2004 Jul; 89(7):777-81. PubMed ID: 15257928
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
