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Journal Abstract Search

304 related items for PubMed ID: 1398296

  • 1. A new mutation in the beta-globin gene (IVS II-850 G-C) found in a Yugoslavian beta-thalassemia heterozygote.
    Jankovic L, Dimovski AJ, Sukarova E, Juricic D, Efremov GD.
    Haematologica; 1992; 77(2):119-21. PubMed ID: 1398296
    [Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. The molecular pathology of beta-thalassemia in Turkey: the Boğaziçi university experience.
    Basak AN.
    Hemoglobin; 2007; 31(2):233-41. PubMed ID: 17486506
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  • 4. Beta-thalassemia syndromes.
    Bank A, Dobkin C.
    Birth Defects Orig Artic Ser; 1987; 23(5A):61-9. PubMed ID: 3689946
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  • 5. 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
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  • 6. [Testing of G----A mutation in position 110 of a minor intron of beta-globin genes in patients with thalassemia in Azerbaijan].
    Fedorov AN, Rasulov EM, Oretskaia TS, Lebedeva IV, Ivanovskaia MG, Shabarova ZA, Limborskaia SA.
    Mol Gen Mikrobiol Virusol; 1990 Jan; (1):18-22. PubMed ID: 2139713
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  • 7. 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 Jan; 82(3):269-80. PubMed ID: 9234571
    [Abstract] [Full Text] [Related]

  • 8. 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
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  • 12. "Silent" nucleotide substitution in codon 24 of a beta+ thalassemia globin gene activates splice site in coding sequence RNA.
    Humphries RK, Ley T, Goldsmith ME, Kantor JA, Cline AC, Nienhuis AW.
    Prog Clin Biol Res; 1983 Nov; 134():123-6. PubMed ID: 6664994
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  • 13. Dominantly Inherited beta-Thalassemia.
    Efremov GD.
    Hemoglobin; 2007 Nov; 31(2):193-207. PubMed ID: 17486503
    [Abstract] [Full Text] [Related]

  • 14. Concomitant inheritance of homozygous alpha-thalassemia-2 with homozygous IVS-I-5 G-C beta gene mutation does not influence the severity of the thalassemic phenotype.
    Beris PH, Darbellay R, Beck D, Oner R.
    Nouv Rev Fr Hematol (1978); 1991 Nov; 33(3):227-30. PubMed ID: 1720237
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  • 15. 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 Nov; 23 Suppl 2():14-21. PubMed ID: 1363706
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  • 16. Beta-, delta beta-thalassemia and Hb lepore among Yugoslav, Bulgarian, Turkish and Albanian.
    Efremov GD.
    Haematologica; 1990 Nov; 75 Suppl 5():31-41. PubMed ID: 2086380
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  • 18. [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
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  • 19. [Frequency of molecular alterations in heterozygous beta-thalassemia in southern Spain and their relation to the hematologic phenotype].
    Molina MA, Romero MJ, Abril E, Delgado I, Cano RM, Garrido F, de Pablos JM, Garrido ML.
    Sangre (Barc); 1994 Aug; 39(4):253-6. PubMed ID: 7985053
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