546 related articles for article (PubMed ID: 12353305)
1. Molecular analysis of beta-thalassemia in South Vietnam.
Svasti S; Hieu TM; Munkongdee T; Winichagoon P; Van Be T; Van Binh T; Fucharoen S
Am J Hematol; 2002 Oct; 71(2):85-8. PubMed ID: 12353305
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. The molecular analysis of beta-thalassemia mutations in Lorestan Province, Iran.
Kiani AA; Mortazavi Y; Zeinali S; Shirkhani Y
Hemoglobin; 2007; 31(3):343-9. PubMed ID: 17654071
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. Molecular heterogeneity of beta-thalassemia in Thailand.
Fukumaki Y; Fucharoen S; Fucharoen G; Okamoto N; Ichinose M; Jetsrisuparb A; Sriroongrueng W; Nopparatana C; Laosombat V; Panich V
Southeast Asian J Trop Med Public Health; 1992; 23 Suppl 2():14-21. PubMed ID: 1363706
[TBL] [Abstract][Full Text] [Related]
8. Molecular spectrum of β-thalassemia mutations in the admixed Venezuelan population, and their linkage to β-globin gene haplotypes.
Bravo-Urquiola M; Arends A; Gómez G; Montilla S; Gerard N; Chacin M; Berbar T; García O; García G; Velasquez D; Castillo O; Krishnamoorthy R
Hemoglobin; 2012; 36(3):209-18. PubMed ID: 22563936
[TBL] [Abstract][Full Text] [Related]
9. Molecular basis of beta-thalassemia minor in Taiwan.
Chang JG; Lin CP; Liu TC; Chiou SS; Chen PH; Lee LS; Chen TP
Int J Hematol; 1994 Jun; 59(4):267-72. PubMed ID: 8086620
[TBL] [Abstract][Full Text] [Related]
10. Prenatal and molecular diagnosis of beta-thalassemia major in Taiwan by naturally and amplified created restriction sites.
Chiou SS; Liu TC; Chang TT; Tseng WP; Sy WD; Chang JG
Int J Hematol; 1993 Dec; 59(1):1-8. PubMed ID: 8161731
[TBL] [Abstract][Full Text] [Related]
11. [Molecular-genetic characteristics of alpha, beta and delta beta-thalassemias in 139 heterozygotes in 56 unrelated Czech and Slovak families (Priority description of 3 beta-thalassemia mutations, an extensive alpha-thalassemia 2 (18+ kb) deletion and a Swiss-type nondeletion hereditary persistence of hemoglobin F)].
Indrák K; Divoký V; Brabec V; Indráková J; Svobodová M; Huisman TH
Vnitr Lek; 1993 Oct; 39(10):969-78. PubMed ID: 7694425
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Genotypic correlation between six common beta-thalassemia mutations and the XmnI polymorphism in the Moroccan population.
Agouti I; Badens C; Abouyoub A; Khattab M; Sayah F; Barakat A; Bennani M
Hemoglobin; 2007; 31(2):141-9. PubMed ID: 17486495
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Impact of beta globin gene mutations on the clinical phenotype of beta thalassemia in India.
Colah R; Nadkarni A; Gorakshakar A; Phanasgaonkar S; Surve R; Subramaniam PG; Bondge N; Pujari K; Ghosh K; Mohanty D
Blood Cells Mol Dis; 2004; 33(2):153-7. PubMed ID: 15315795
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. The molecular pathology of beta-thalassemia in Turkey: the Boğaziçi university experience.
Basak AN
Hemoglobin; 2007; 31(2):233-41. PubMed ID: 17486506
[TBL] [Abstract][Full Text] [Related]
18. Molecular basis of β-thalassemia in the United Arab Emirates.
Baysal E
Hemoglobin; 2011; 35(5-6):581-8. PubMed ID: 22074124
[TBL] [Abstract][Full Text] [Related]
19. Molecular characterization of sickle cell anemia in the Northern Brazilian state of Pará.
De Lemos Cardoso G; Guerreiro JF
Am J Hum Biol; 2010; 22(5):573-7. PubMed ID: 20737602
[TBL] [Abstract][Full Text] [Related]
20. Prenatal diagnosis of beta-thalassaemia by reverse dot-blot hybridization.
Winichagoon P; Saechan V; Sripanich R; Nopparatana C; Kanokpongsakdi S; Maggio A; Fucharoen S
Prenat Diagn; 1999 May; 19(5):428-35. PubMed ID: 10360511
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
