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PUBMED FOR HANDHELDS

Journal Abstract Search


193 related items for PubMed ID: 4685506

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  • 7. [Prenatal biochemical diagnosis of Tay-Sachs disease].
    Rozenfel'd EL, Tsvetkova IV, Kozina AB, Rozovskiĭ IS, Kovrigina NG.
    Vopr Med Khim; 1972; 18(4):445-6. PubMed ID: 4661856
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  • 8. [Tay-Sachs disease: prenatal detection and diagnosis].
    Delvin EE, Scriver CR, Pottier A, Clow CL, Goldman H.
    Union Med Can; 1972 Apr; 101(4):683-8. PubMed ID: 5062350
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  • 11. [GM2 gangliosidosis diagnosis and carriers detection by fractionation of N-acetyl-beta-D-hexosaminidase by electrophoresis on cellulose acetate gel (author's transl)].
    Pampols T, Girós ML, González Sastre F, Sabater J.
    An Esp Pediatr; 1977 Oct; 10(10):695-704. PubMed ID: 607830
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  • 12. Diagnosis of Tay-Sachs disease by hexosaminidase activity in leukocytes and amniotic fluid cells.
    Padeh B, Navon R.
    Isr J Med Sci; 1971 Feb; 7(2):259-63. PubMed ID: 5560980
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  • 14. Letter: Prenatal diagnosis of Tay-Sachs disease.
    Ellis RB, Ikonne JU, Patrick AD, Stephens R, Willcox P.
    Lancet; 1973 Nov 17; 2(7838):1144-5. PubMed ID: 4128028
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  • 20. Editorial: Heterozygote screening--a social challenge.
    Kaback MM.
    N Engl J Med; 1973 Nov 15; 289(20):1090-1. PubMed ID: 4742226
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