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  • Title: [Clinical and molecular problems in polycystic kidneys].
    Author: Kucerová M, Zdárský E, Gregor V, Merta M, Kapras J, Dolanská M.
    Journal: Cas Lek Cesk; 1990 Jan 12; 129(2):36-9. PubMed ID: 1970760.
    Abstract:
    The authors examined, using nephrological, genealogical and molecular genetic methods, 85 subjects from 19 families with autosomal dominant heredity of polycystic kidney disease. Using the probe 3HVR alpha-globin and restriction endonuclease Pvu II, the authors assessed 95% informative families in the given group and the reliability of the diagnosis was also 95%. The authors tested the homogeneity of the disease in the Czech population and the applicability of the mentioned probe and endonuclease for molecular genetic testing of our population.
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