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Journal Abstract Search

204 related items for PubMed ID: 4982583

  • 1. The starch gel quantitative electrophoresis of haemoglobin as screening in the thalassaemia syndromes.
    Ricco G, Gallo E, Mazza U, Bianco G, Prato V.
    Acta Haematol; 1969; 42(2):99-105. PubMed ID: 4982583
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  • 2. [Hemoglobin of the African newborn infant. Results of an investigation in Senegal].
    Oudart JL, Diadhiou F, Sarrat H, Satgé P.
    Ann Pediatr (Paris); 1968 Dec 02; 15(12):773-81. PubMed ID: 4894442
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  • 3. [The hemoglobins. I. Structure of the normal and abnormal hemoglobins].
    Piguet H.
    Presse Med (1893); 1968 Mar 02; 76(11):519-21. PubMed ID: 5646256
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  • 7. An assessment of techniques suitable for the diagnosis of sickle-cell disease and haemoglobin C disease in cord blood samples.
    Yaswon GI, Huntsman RG, Metters JS.
    J Clin Pathol; 1970 Sep 02; 23(6):533-7. PubMed ID: 5476880
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  • 9. Some problems of hemoglobin patterns in different thalassemic syndromes showing the heterogeneity of beta-thalassemia genes.
    Aksoy M, Erdem S.
    Ann N Y Acad Sci; 1969 Nov 20; 165(1):13-24. PubMed ID: 5260139
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  • 11. Antenatal diagnosis of haemoglobinopathies by Biorex chromatography of haemoglobin.
    Blouquit Y, Beuzard Y, Varnavides L, Chabret C, Dumez Y, John PN, Rodeck C, White JM.
    Br J Haematol; 1982 Jan 20; 50(1):7-15. PubMed ID: 6173058
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  • 16. Pre- and postnatal diagnosis of the hemoglobinopathies.
    Alter BP.
    Birth Defects Orig Artic Ser; 1981 Jan 20; 17(1):181-99. PubMed ID: 6169382
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