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Journal Abstract Search

85 related items for PubMed ID: 2430864

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  • 4. The polymorphism of human fetal hemoglobin.
    Huisman TH.
    Birth Defects Orig Artic Ser; 1982; 18(7):83-99. PubMed ID: 6186316
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  • 5. Interaction between deletion delta-thalassemia and beta zero-thalassemia (codon 39 nonsense mutation) in a Sardinian family.
    Galanello R, Podda A, Melis MA, Monne M, Cao A.
    Prog Clin Biol Res; 1989; 316B():113-21. PubMed ID: 2482492
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  • 6. Clinical and hematologic phenotype of homozygous beta+ (high A2)-thalassemia with low Hb F.
    Kattamis CA, Metaxotou-Mavromati A, Mitsioni A, Kanavakis E.
    Birth Defects Orig Artic Ser; 1987; 23(5A):303-7. PubMed ID: 2446674
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  • 8. A non-deletion hereditary persistence of fetal hemoglobin (HPFH) determinant not linked to the beta-globin gene complex.
    Thein SL, Weatherall DJ.
    Prog Clin Biol Res; 1989; 316B():97-111. PubMed ID: 2482508
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  • 9. Homozygosity for a new type of G gamma (A gamma delta beta)zero-thalassemia in a Malaysian male.
    George E, Faridah K, Trent RJ, Padanilam BJ, Huang HJ, Huisman TH.
    Hemoglobin; 1986; 10(4):353-63. PubMed ID: 2427478
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  • 10. Sequence variations in the 3' A gamma enhancer are silent polymorphisms.
    Ragusa A, Lombardo M, Lombardo T, Beldjord C, Nagel RL, Elion J, Labie D, Krishnamoorthy R.
    Prog Clin Biol Res; 1989; 316B():409-17. PubMed ID: 2482506
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  • 11. Genetic heterogeneity of beta zero-thalassemia intermedia in Southern Sardinia.
    Cacace E, Frigerio R, Olla N, Sole G, Mela Q, Perpignano G, Carcassi U.
    Haematologica; 1985; 70(2):95-100. PubMed ID: 2408975
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  • 14. Hematological phenotype of carriers of deletion alpha-thalassemia according to the alpha-globin genotype.
    Galanello R, Paglietti E, Giagu N, Melis MA, Scalas MT, Cao A.
    Haematologica; 1985; 70(3):191-8. PubMed ID: 3932145
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  • 16. [Intermediate beta thalassemia of the delta-beta (0)/(delta-beta) (0) genotype. Report of a case].
    Sáenz GF, Carrillo JM, Mora L, Chaves M, Rojas LG, Jiménez R, Jiménez J, Montero AG.
    Sangre (Barc); 1984; 29(4-A):467-72. PubMed ID: 6209815
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  • 18. Molecular characterization of delta beta-thalassemia and hereditary persistence of fetal hemoglobin in the Indian population.
    Nadkarni A, Wadia M, Gorakshakar A, Kiyama R, Colah RB, Mohanty D.
    Hemoglobin; 2008; 32(5):425-33. PubMed ID: 18932066
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  • 20. Genetic and molecular analysis of mild forms of homozygous beta-thalassemia.
    Weatherall DJ, Wainscoat JS, Thein SL, Old JM, Wood WG, Higgs DR, Clegg JB.
    Ann N Y Acad Sci; 1985; 445():68-80. PubMed ID: 2409878
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