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Journal Abstract Search

101 related items for PubMed ID: 103586

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  • 2. Complementation analysis of beta-galactosidase deficiency by means of histochemical method.
    Minami R, Wagatsuma K, Ishikawa Y, Watanabe M, Kusano T, Nakao T, Tsugawa S.
    Tohoku J Exp Med; 1985 Jun; 146(2):181-7. PubMed ID: 3927517
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  • 4. The complementation of beta-galactosidase in fused cells of mucolipidosis II with another variants of beta-galactosidase deficiency using new single cell enzyme assay.
    Okada S, Kato T, Yabuuchi H, Okada Y.
    Biochem Biophys Res Commun; 1979 May 28; 88(2):559-62. PubMed ID: 111672
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  • 5. Morquio B syndrome: a primary defect in beta-galactosidase.
    van der Horst GT, Kleijer WJ, Hoogeveen AT, Huijmans JG, Blom W, van Diggelen OP.
    Am J Med Genet; 1983 Oct 28; 16(2):261-75. PubMed ID: 6418007
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  • 10. Distribution of the adult lactase phenotypes--lactose absorber and malabsorber--in a group of 131 army recruits.
    Cuddenec Y, Delbrück H, Flatz G.
    Gastroenterol Clin Biol; 1982 Oct 28; 6(10):776-9. PubMed ID: 6816656
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  • 12. Complementation, cross correction, and drug correction studies of combined beta-galactosidase neuraminidase deficiency in human fibroblasts.
    Strisciuglio P, Creek KE, Sly WS.
    Pediatr Res; 1984 Feb 28; 18(2):167-71. PubMed ID: 6422434
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  • 13. Genetics of lactose digestion in humans.
    Flatz G.
    Adv Hum Genet; 1987 Feb 28; 16():1-77. PubMed ID: 3105269
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  • 14. Distribution of human adult lactose phenotypes in Egypt.
    Hussein L, Flatz SD, Kühnau W, Flatz G.
    Hum Hered; 1982 Feb 28; 32(2):94-9. PubMed ID: 6807827
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  • 15. Distribution of the adult lactase phenotypes in Turkey.
    Flatz G, Henze HJ, Palabiyikoglu E, Dagalp K, Türkkan T.
    Trop Geogr Med; 1986 Sep 28; 38(3):255-8. PubMed ID: 3092418
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  • 17. Interspecific genetic complementation analysis of human and sheep fibroblasts with beta-galactosidase deficiency.
    Ahern-Rindell AJ, Murnane RD, Prieur DJ.
    Somat Cell Mol Genet; 1989 Nov 28; 15(6):525-33. PubMed ID: 2512653
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