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Journal Abstract Search

148 related items for PubMed ID: 6240199

  • 1.
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  • 2. Prenatal diagnosis for Tay-Sachs disease using chorionic villus sampling.
    Grebner EE, Jackson LG.
    Prenat Diagn; 1985; 5(5):313-20. PubMed ID: 2933645
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  • 4. Use of 4-methylumbelliferyl-6-sulpho-2-acetamido-2-deoxy-beta- D-glucopyranoside for prenatal diagnosis of Tay-Sachs disease using chorionic villi.
    Grebner EE, Wenger DA.
    Prenat Diagn; 1987 Jul; 7(6):419-23. PubMed ID: 2958791
    [Abstract] [Full Text] [Related]

  • 5. First trimester prenatal diagnosis of Tay-Sachs disease using the sulfated synthetic substrate for hexosaminidase A.
    Callahan JW, Archibald A, Skomorowski MA, Shuman C, Clarke JT.
    Clin Biochem; 1990 Dec; 23(6):533-6. PubMed ID: 2149678
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  • 6. Prenatal diagnosis of Tay-Sachs disease with heat-labile beta-hexosaminidase B.
    Momoi T, Kikuchi K, Shigematsu Y, Sudo M, Tanioka K.
    Clin Chim Acta; 1983 Oct 14; 133(3):331-4. PubMed ID: 6226459
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  • 7. Prenatal diagnosis of Tay-Sachs disease. Reflectometry of hexosaminidase A, B, and C/S bands on zymograms.
    Kustermann-Kuhn B, Harzer K.
    Hum Genet; 1983 Oct 14; 65(2):172-5. PubMed ID: 6228513
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  • 8. Rapid detection of fetal Mendelian disorders: Tay-Sachs disease.
    Guetta E, Peleg L.
    Methods Mol Biol; 2008 Oct 14; 444():147-59. PubMed ID: 18425478
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  • 10. Prenatal diagnosis of metabolic diseases on chorionic villi obtained before the ninth week of pregnancy.
    Minelli A, Piantanida M, Simoni G, Rossella F, Romitti L, Brambati B, Danesino C.
    Prenat Diagn; 1992 Nov 14; 12(11):959-63. PubMed ID: 1362984
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  • 12. Enzyme studies in GM2 gangliosidiosis, and their application in prenatal diagnosis.
    Kaur M, Verma IC.
    Indian J Pediatr; 1995 Nov 14; 62(4):485-9. PubMed ID: 10829910
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  • 13. Electrophoresis with direct fluorometry for the diagnosis of Tay-Sachs disease and carriers.
    Saruwatari AS, Schmidt BJ, Diament AJ.
    Clin Chem; 1986 Jun 14; 32(6):1232-3. PubMed ID: 2940030
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  • 14. [Prenatal diagnosis of mannosidosis using chorion villi].
    Petushkova NA, Tsvetkova IV, Fuks MA, Doronin GL, Iakubovich DV.
    Vopr Med Khim; 1987 Jun 14; 33(4):99-101. PubMed ID: 2958965
    [Abstract] [Full Text] [Related]

  • 15. Adult-onset GM2 gangliosidosis diagnosed in a fetus.
    Navon R, Sandbank U, Frisch A, Baram D, Adam A.
    Prenat Diagn; 1986 Jun 14; 6(3):169-76. PubMed ID: 2941730
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  • 17. Hereditary heat-labile hexosaminidase B: its implication for recognizing Tay-Sachs genotypes.
    Navon R, Nutman J, Kopel R, Gaber L, Gadoth N, Goldman B, Nitzan M.
    Am J Hum Genet; 1981 Nov 14; 33(6):907-15. PubMed ID: 6459736
    [Abstract] [Full Text] [Related]

  • 18. Frequency of hexosaminidase A variant alleles among Ashkenazi Jews and prenatal diagnosis of GM2 gangliosidosis.
    Navon R, Adam A.
    Am J Hum Genet; 1985 Sep 14; 37(5):1031-3. PubMed ID: 2931975
    [No Abstract] [Full Text] [Related]

  • 19. Prenatal Diagnosis of Tay-Sachs Disease.
    Zhang J, Chen H, Kornreich R, Yu C.
    Methods Mol Biol; 2019 Sep 14; 1885():233-250. PubMed ID: 30506202
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