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Journal Abstract Search

317 related items for PubMed ID: 8086620

  • 1.
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  • 2. 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
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  • 3. 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 Dec; 43(4):237-41. PubMed ID: 9852674
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  • 5. Molecular characterization of beta-thalassemia in Egyptians.
    Hussein IR, Temtamy SA, el-Beshlawy A, Fearon C, Shalaby Z, Vassilopoulos G, Kazazian HH.
    Hum Mutat; 1993 Dec; 2(1):48-52. PubMed ID: 8477263
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  • 9. 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 Dec; 30(1):15-21. PubMed ID: 16540410
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  • 10. 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 Dec; 31(1):63-9. PubMed ID: 17365006
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  • 12. The molecular pathology of beta-thalassemia in Turkey: the Boğaziçi university experience.
    Basak AN.
    Hemoglobin; 2007 Dec; 31(2):233-41. PubMed ID: 17486506
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  • 13. Dominantly Inherited beta-Thalassemia.
    Efremov GD.
    Hemoglobin; 2007 Dec; 31(2):193-207. PubMed ID: 17486503
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  • 14. Molecular characterization of deletional forms of beta-thalassemia in Taiwan.
    Peng CT, Liu SC, Chiou SS, Kuo PL, Shih MC, Chang JY, Chang JG.
    Ann Hematol; 2003 Jan; 82(1):33-6. PubMed ID: 12574962
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  • 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 Jan; 41(1):56-9. PubMed ID: 18381244
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  • 18. Rapid detection of beta-Thalassemia alleles in Egypt using naturally or amplified created restriction sites and direct sequencing: a step in disease control.
    Hussein G, Fawzy M, Serafi TE, Ismail EF, Metwally DE, Saber MA, Giansily M, Schved JF, Pissard S, Martinez PA.
    Hemoglobin; 2007 Jan; 31(1):49-62. PubMed ID: 17365005
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  • 19. 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 Jan; 26 Suppl 1():229-34. PubMed ID: 8629112
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  • 20. Spectrum of beta-thalassaemia mutations in transfusion dependent thalassaemia patients: practical implications in prenatal diagnosis.
    George E, George R, Ariffin WA, Mokhtar AB, Azman ZA, Sivagengei K.
    Med J Malaysia; 1993 Sep; 48(3):325-9. PubMed ID: 8183146
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