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Journal Abstract Search

172 related items for PubMed ID: 4776531

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  • 2. Genetic variants of Tay-Sachs disease: Tay-Sachs disease and Sandhoff's disease in French Canadians, juvenile Tay-Sachs disease in Lebanese Canadians, and a Tay-Sachs screening program in the French-Canadian population.
    Andermann E, Scriver CR, Wolfe LS, Dansky L, Andermann F.
    Prog Clin Biol Res; 1977; 18():161-88. PubMed ID: 601075
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  • 4. [Enzymatic studies on the blood of carriers of a Tay-Sachs disease variant (variant O)].
    Harzer K, Sandhoff K, Schall H, Kollmann F.
    Klin Wochenschr; 1971 Nov 01; 49(21):1189-91. PubMed ID: 5124584
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  • 6. Enzymic differentiation between different types of Tay-Sachs disease of similar clinical appearance.
    Clausen J, Melchior JC, Paerregaard P.
    Eur Neurol; 1972 Nov 01; 7(1):56-64. PubMed ID: 4336274
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  • 8. Tay-Sachs disease in a Moroccan Jewish family: a possible new mutation.
    Bach G, Navon R, Zeigler M, Beyth Y, Porter B, Cohen MM.
    Isr J Med Sci; 1976 Dec 01; 12(12):1432-9. PubMed ID: 1017941
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  • 16. Basic findings and current developments in sphingolipidoses.
    Pilz H, Heipertz R, Seidel D.
    Hum Genet; 1979 Mar 12; 47(2):113-34. PubMed ID: 108196
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  • 17. Tay-Sachs disease heterozygote detection: a quality control study.
    Kaback MM, Shapiro LJ, Hirsch P, Roy C.
    Prog Clin Biol Res; 1977 Mar 12; 18():267-79. PubMed ID: 601080
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  • 18. [Problems in the diagnosis of metachromatic leukodystrophy by arylsulfatase-A assay in white blood cells. Genetic study of normal enzyme values in 64 mother and child pairs (author's transl)].
    Harzer K, Gussmann KI.
    Arch Psychiatr Nervenkr (1970); 1981 Mar 12; 229(4):291-304. PubMed ID: 6111988
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  • 20. Carrier screening techniques for Tay-Sachs and other lysosomal storage diseases.
    Kolodny EH.
    Prog Clin Biol Res; 1977 Mar 12; 18():213-9. PubMed ID: 601077
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