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Journal Abstract Search

112 related items for PubMed ID: 49545

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  • 4. Genetic complementation analysis in somatic cell hybrids of alpha-L-iduronidase deficient cells.
    Wehnert M, Machill G, Petruschka L.
    Hum Genet; 1985; 69(3):287. PubMed ID: 3920140
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  • 5. The clinical spectrum of alpha-L-iduronidase deficiency.
    Roubicek M, Gehler J, Spranger J.
    Am J Med Genet; 1985 Mar; 20(3):471-81. PubMed ID: 3922223
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  • 12. Heparan sulfate and dermatan sulfate from the liver of a patient with Hurler syndrome: high performance liquid chromatography of their degradation products after incubation with alpha-L-iduronidase-deficient fibroblasts.
    Minami R, Fujibayashi S, Igarashi C, Ishikawa Y, Wagatsuma K, Nakao T, Tsugawa S.
    Clin Chim Acta; 1984 Feb 28; 137(2):179-87. PubMed ID: 6231139
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  • 14. A new phenotypic variant of alpha-L-iduronidase deficiency.
    Kohn G, Bach G, Lasch E, Massri ME, Legum C, Cohen MM.
    Monogr Hum Genet; 1978 Feb 28; 10():7-10. PubMed ID: 723907
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  • 16. Canine alpha-L-iduronidase deficiency. A model of mucopolysaccharidosis I.
    Shull RM, Munger RJ, Spellacy E, Hall CW, Constantopoulos G, Neufeld EF.
    Am J Pathol; 1982 Nov 28; 109(2):244-8. PubMed ID: 6215865
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  • 17. A canine model of human alpha-L-iduronidase deficiency.
    Spellacy E, Shull RM, Constantopoulos G, Neufeld EF.
    Proc Natl Acad Sci U S A; 1983 Oct 28; 80(19):6091-5. PubMed ID: 6412235
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  • 19. Letter: Chondroitinsulphaturia with alpha-L-iduronidase deficiency.
    Babarik A, Benson PF, Dean MF, Muir H.
    Lancet; 1974 Aug 24; 2(7878):464-5. PubMed ID: 4136880
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