119 related articles for article (PubMed ID: 7577658)
1. Beta-thalassaemia unlinked to the beta-globin gene interacts with sickle-cell trait in a Portuguese family.
Pacheco P; Peres MJ; Faustino P; Pischedda C; Gonçalves J; Carvajales-Ramos M; Seixas T; Martins MC; Moi P; Lavinha J
Br J Haematol; 1995 Sep; 91(1):85-9. PubMed ID: 7577658
[TBL] [Abstract][Full Text] [Related]
2. Beta-thalassemia unlinked to the beta-globin gene in an English family.
Thein SL; Wood WG; Wickramasinghe SN; Galvin MC
Blood; 1993 Aug; 82(3):961-7. PubMed ID: 8101733
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Dominantly inherited beta thalassaemia intermedia caused by a new single nucleotide deletion in exon 2 of the beta globin gene: Hb morgantown (beta91 CTG>CG).
Luo HY; Tang W; Eung SH; Coad JE; Canfield P; Keller F; Crowell EH; Steinberg MH; Chui DH
J Clin Pathol; 2005 Oct; 58(10):1110-2. PubMed ID: 16189162
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. A case of non-beta-globin gene linked beta thalassaemia in a Dutch family with two additional alpha-gene defects: the common -alpha3.7 deletion and the rare IVS1-116 (A-->G) acceptor splice site mutation.
Giordano PC; Harteveld CL; Haak HL; Batelaan D; van Delft P; Plug RJ; Emonts M; Zanardini R; Bernini LF
Br J Haematol; 1998 Nov; 103(2):370-6. PubMed ID: 9827907
[TBL] [Abstract][Full Text] [Related]
7. The triplicated alpha-globin gene locus in beta-thalassaemia heterozygotes: clinical, haematological, biosynthetic and molecular studies.
Traeger-Synodinos J; Kanavakis E; Vrettou C; Maragoudaki E; Michael T; Metaxotou-Mavromati A; Kattamis C
Br J Haematol; 1996 Dec; 95(3):467-71. PubMed ID: 8943886
[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. [The molecular basis of dominantly inherited beta-thalassemia].
Faustino P; Barbot J; Gonçalves J; Peres MJ; Lavinha J
Acta Med Port; 1999; 12(7-11):293-6. PubMed ID: 10707468
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Evaluation of high performance liquid chromatography (HPLC) pattern and prevalence of beta-thalassaemia trait among sickle cell disease patients in Lagos, Nigeria.
Adeyemo T; Ojewunmi O; Oyetunji A
Pan Afr Med J; 2014; 18():71. PubMed ID: 25400838
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. Possible factors influencing the haemoglobin and fetal haemoglobin levels in patients with beta-thalassaemia due to a homozygosity for the IVS-I-6 (T-->C) mutation.
Efremov DG; Dimovski AJ; Baysal E; Ye Z; Adekile AD; Ribeiro ML; Schiliro G; Altay C; Gürgey A; Efremov GD
Br J Haematol; 1994 Apr; 86(4):824-30. PubMed ID: 7522523
[TBL] [Abstract][Full Text] [Related]
15. Initiation codon mutation (ATG --> ATA) of the beta-globin gene causing beta-thalassemia in a Swedish family.
Landin B; Rudolphi O; Ek B
Am J Hematol; 1995 Mar; 48(3):158-62. PubMed ID: 7864023
[TBL] [Abstract][Full Text] [Related]
16. Mouse microcytic anaemia caused by a defect in the gene encoding the globin enhancer-binding protein NF-E2.
Peters LL; Andrews NC; Eicher EM; Davidson MB; Orkin SH; Lux SE
Nature; 1993 Apr; 362(6422):768-70. PubMed ID: 8469289
[TBL] [Abstract][Full Text] [Related]
17. Haplotypes linked to three rare beta-thalassemia mutations, originally reported in Tunisia.
Bibi A; Messaoud T; Fattoum S
Hemoglobin; 2006; 30(2):175-81. PubMed ID: 16798642
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. beta+-Thalassaemia, Haemoglobin S and Hereditary elliptocytosis in a Zairian Family. Ischaemic costal necroses in a child with sickle cell beta+-Thalassaemia.
Ros G; Seynhaeve V; Fiasse L
Acta Haematol; 1976; 56(4):241-52. PubMed ID: 826082
[TBL] [Abstract][Full Text] [Related]
20. A novel beta-thalassaemia mutation in the 5' untranslated region of the beta-globin gene.
Athanassiadou A; Papachatzopoulou A; Zoumbos N; Maniatis GM; Gibbs R
Br J Haematol; 1994 Oct; 88(2):307-10. PubMed ID: 7803275
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
