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PUBMED FOR HANDHELDS

Journal Abstract Search


125 related items for PubMed ID: 204112

  • 21. Galactosaemia and the problem of galactose toxicity.
    Schwarz V.
    Biochem Soc Trans; 1975; 3(2):234-8. PubMed ID: 165990
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  • 22. [Gene frequency of hereditary galactosemia with reference to the Duarte variant].
    Kaloud H, Sitzmann FC.
    Z Kinderheilkd; 1972; 113(3):205-14. PubMed ID: 4674437
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  • 31. [Activity of enzymes of galactose metabolism in so-called congenital cataract (author's transl)].
    Kaloud H, Sitzmann FC, Schenker H, Prestele H.
    Dtsch Med Wochenschr; 1975 Apr 18; 100(16):873-6. PubMed ID: 164335
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  • 32. Polymorphism of galactose-1-phosphate uridyltransferase in the Albanian and Croatian settlements of Molise (Italy).
    Vaccaro AM, Mandara I, Ciaffoni F, Biondi G.
    Anthropol Anz; 1984 Dec 18; 42(4):307-14. PubMed ID: 6099092
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  • 34. Human erythrocyte galactokinase and galactose-1-phosphate uridylyltransferase: a population survey.
    Tedesco TA, Miller KL, Rawnsley BE, Mennuti MT, Spielman RS, Mellman WJ.
    Am J Hum Genet; 1975 Nov 18; 27(6):737-47. PubMed ID: 173184
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  • 39. An unusual form of galactosemia: studies on erythrocytes and hair roots.
    de Bruyn CH, Oei TL, Monnens LA, Trijbels JM.
    Clin Genet; 1978 Jan 18; 13(1):8-16. PubMed ID: 203421
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  • 40. Genetic basis of transferase-deficient galactosaemia in Ireland and the population history of the Irish Travellers.
    Murphy M, McHugh B, Tighe O, Mayne P, O'Neill C, Naughten E, Croke DT.
    Eur J Hum Genet; 1999 Jul 18; 7(5):549-54. PubMed ID: 10439960
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