209 related articles for article (PubMed ID: 10707468)
1. [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]
2. 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]
3. Identification of a novel frameshift mutation at codon 53 (-T) in the beta-globin gene causing dominantly inherited beta-thalassemia in a Chinese Miao family.
Yi P; Yu F; Huang S; Zhong C; Li Q; Yang Y; Zhang W; Xiao C; Xu X
Blood Cells Mol Dis; 2008; 41(1):56-9. PubMed ID: 18381244
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. 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; 70(4):269-77. PubMed ID: 12210807
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Spectrum of beta thalassemia mutations and HbF levels in the heterozygous Moroccan population.
Lemsaddek W; Picanço I; Seuanes F; Mahmal L; Benchekroun S; Khattab M; Nogueira P; Osório-Almeida L
Am J Hematol; 2003 Jul; 73(3):161-8. PubMed ID: 12827652
[TBL] [Abstract][Full Text] [Related]
9. Beta-globin cluster haplotypes in normal individuals and beta(0)39-thalassemia carriers from Sardinia, Italy.
Piras I; Vona G; Falchi A; Latini V; Ristaldi S; Vacca L; Varesi L; Calò CM
Am J Hum Biol; 2005; 17(6):765-72. PubMed ID: 16254903
[TBL] [Abstract][Full Text] [Related]
10. [Molecular diagnosis in a Korean family with thalassemia intermedia due to co-inheritance of triplicated alpha-globin genes (alphaalpha/alphaalphaalpha(anti 3.7)) and beta-thalassemia trait (IVS-II-1 G-->A)].
Chen M; Han JY; Sun Q; Kim IH; Ren Z; Huang S; Zeng Y
Zhonghua Xue Ye Xue Za Zhi; 2000 Apr; 21(4):195-7. PubMed ID: 11876981
[TBL] [Abstract][Full Text] [Related]
11. Silent thalassemias: genotypes and phenotypes.
Bianco I; Cappabianca MP; Foglietta E; Lerone M; Deidda G; Morlupi L; Grisanti P; Ponzini D; Rinaldi S; Graziani B
Haematologica; 1997; 82(3):269-80. PubMed ID: 9234571
[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. First Spanish case of thalassemia major due to a compound heterozygosity for the IVS-II-848 (C --> A) and codon 39 (C --> T) mutations of the beta-globin gene.
Ropero P; Villegas A; Muñoz J; Briceño O; Mora A; Salvador M; Polo M; González FA
Hemoglobin; 2006; 30(1):15-21. PubMed ID: 16540410
[TBL] [Abstract][Full Text] [Related]
14. Asymptomatic homozygous deletional beta(0)-thalassemia in an African individual.
Faustino P; Reis AB; Feliciano H; Ferrão L; Pereira P; Picanço I; Miranda A; Seixas T; Romão L; Júnior EC; Lavinha J
Am J Hematol; 2002 Jul; 70(3):232-6. PubMed ID: 12111769
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. [Molecular diagnosis of beta-thalassemia intermedia].
Chen J; Liu W; Chen M
Zhonghua Yi Xue Za Zhi; 1997 Aug; 77(8):575-8. PubMed ID: 9772460
[TBL] [Abstract][Full Text] [Related]
17. The clinical significance of the spectrum of interactions of CAP+1 (A-->C), a silent beta-globin gene mutation, with other beta-thalassemia mutations and globin gene modifiers in north Indians.
Garewal G; Das R; Awasthi A; Ahluwalia J; Marwaha RK
Eur J Haematol; 2007 Nov; 79(5):417-21. PubMed ID: 17900295
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Phenotypes of individuals with a beta thal classical allele associated either with a beta thal silent allele or with alpha globin gene triplication.
Bianco I; Lerone M; Foglietta E; Deidda G; Cappabianca MP; Morlupi L; Ponzini D; Grisanti P; Di Biagio P; Amato A; Mezzabotta M; Graziani B
Haematologica; 1997; 82(5):513-25. PubMed ID: 9407714
[TBL] [Abstract][Full Text] [Related]
20. Double heterozygosity for the codon beta 39 C-to-T nonsense mutation and a triplicate alpha-globin gene locus can cause "dominantly" inherited beta-thalassemia intermedia.
Rhodes SL; Plonczynski M; Harrell A; Li J; Safaya S; Files JC; Steinberg MH
Am J Med Sci; 1999 May; 317(5):341-5. PubMed ID: 10334122
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
