358 related articles for article (PubMed ID: 17706040)
1. [Molecular analysis of beta-thalassemia intermedia in Guangdong Province].
Zhang L; Ou XB; Yu YP
Zhongguo Dang Dai Er Ke Za Zhi; 2007 Aug; 9(4):358-60. PubMed ID: 17706040
[TBL] [Abstract][Full Text] [Related]
2. [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]
3. [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]
4. 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]
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-globin gene mutations among thalassemia patients in the West Bank region of Palestine.
Darwish HM; El-Khatib FF; Ayesh S
Hemoglobin; 2005; 29(2):119-32. PubMed ID: 15921164
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. Analysis of beta-thalassemia mutations and beta-locus control region hypersensitive sites 2, 3 and 4 in southern Thailand.
Sriroongrueng W; Schleiemacher E; Panich V; Nopparatana C; Saechan V; Laosombat V; Pornpatkul M; Fukumaki Y
Southeast Asian J Trop Med Public Health; 1997; 28 Suppl 3():120-7. PubMed ID: 9640613
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. [The prevalence of beta-thalassemia heterozygotes compound alpha-thalassemia in Guangdong district].
Han J; Zeng R; Hu B
Zhonghua Xue Ye Xue Za Zhi; 2001 Oct; 22(10):514-6. PubMed ID: 11769674
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Molecular diagnosis of patients with beta-thalassemia major in central Taiwan by amplified created restriction site analysis.
Peng CT; Wu JY; Tsai CH; Tsai FJ; Chang JG
J Hum Genet; 1998; 43(4):237-41. PubMed ID: 9852674
[TBL] [Abstract][Full Text] [Related]
14. Molecular basis of thalassemia intermedia in Iran.
Akbari MT; Izadi P; Izadyar M; Kyriacou K; Kleanthous M
Hemoglobin; 2008; 32(5):462-70. PubMed ID: 18932071
[TBL] [Abstract][Full Text] [Related]
15. Study of beta-Thalassemia mutations using the polymerase chain reaction-amplification refractory mutation system and direct DNA sequencing techniques in a group of Egyptian Thalassemia patients.
El-Gawhary S; El-Shafie S; Niazi M; Aziz M; El-Beshlawy A
Hemoglobin; 2007; 31(1):63-9. PubMed ID: 17365006
[TBL] [Abstract][Full Text] [Related]
16. [Analysis of RFLP haplotypes in the beta-globin gene cluster and the identification of beta-thalassemia genes in patients from Guangdong Province].
Li J
Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1992 Feb; 14(1):42-5. PubMed ID: 1350518
[TBL] [Abstract][Full Text] [Related]
17. [A rare transcription mutation (-90 C-->T) in a Chinese family with beta-thalassemia].
Li WJ; Lao XW; Jai SQ; Liang FA; Mo QH; Ma JY; Xu XM
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Dec; 20(6):468-70. PubMed ID: 14669211
[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. 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]
20. The spectrum of beta-thalassemia mutations in southern Thailand.
Nopparatana C; Panich V; Saechan V; Sriroongrueng V; Nopparatana C; Rungjeadpha J; Pornpatkul M; Laosombat V; Fukumaki Y
Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():229-34. PubMed ID: 8629112
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]