BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

152 related articles for article (PubMed ID: 6240199)

  • 1. First-trimester prenatal diagnosis of Tay-Sachs disease.
    Grabowski GA; Kruse JR; Goldberg JD; Chockkalingam K; Gordon RE; Blakemore KJ; Mahoney MJ; Desnick RJ
    Am J Hum Genet; 1984 Nov; 36(6):1369-78. PubMed ID: 6240199
    [TBL] [Abstract][Full Text] [Related]  

  • 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
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Prenatal Tay-Sachs diagnosis by chorionic villi sampling.
    Lancet; 1983 Jul; 2(8344):286-7. PubMed ID: 6135112
    [No Abstract]   [Full Text] [Related]  

  • 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
    [TBL] [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
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 133(3):331-4. PubMed ID: 6226459
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 65(2):172-5. PubMed ID: 6228513
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Rapid detection of fetal Mendelian disorders: Tay-Sachs disease.
    Guetta E; Peleg L
    Methods Mol Biol; 2008; 444():147-59. PubMed ID: 18425478
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Prenatal diagnosis of atypical Tay-Sachs disease by chorionic villi sampling.
    Besançon AM; Belon JP; Castelnau L; Dumez Y; Poenaru L
    Prenat Diagn; 1984; 4(5):365-70. PubMed ID: 6504850
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 12(11):959-63. PubMed ID: 1362984
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Prenatal diagnosis of Tay-Sachs disease: studies on the reliability of hexosaminidase levels in amniotic fluid.
    Grebner EE; Jackson LG
    Am J Obstet Gynecol; 1979 Jul; 134(5):547-50. PubMed ID: 453293
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Enzyme studies in GM2 gangliosidiosis, and their application in prenatal diagnosis.
    Kaur M; Verma IC
    Indian J Pediatr; 1995; 62(4):485-9. PubMed ID: 10829910
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Electrophoresis with direct fluorometry for the diagnosis of Tay-Sachs disease and carriers.
    Saruwatari AS; Schmidt BJ; Diament AJ
    Clin Chem; 1986 Jun; 32(6):1232-3. PubMed ID: 2940030
    [No Abstract]   [Full Text] [Related]  

  • 14. [Prenatal diagnosis of mannosidosis using chorion villi].
    Petushkova NA; Tsvetkova IV; Fuks MA; Doronin GL; Iakubovich DV
    Vopr Med Khim; 1987; 33(4):99-101. PubMed ID: 2958965
    [TBL] [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; 6(3):169-76. PubMed ID: 2941730
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Diagnosis of Tay-Sachs disease by estimation of beta-N-acetylhexosaminidase activity using a radiolabeled hyaluronic acid-derived trisaccharide substrate.
    Yutaka T; Kato T; Midorikawa M; Doke M; Okada S; Yabuuchi H
    Clin Chim Acta; 1984 Feb; 137(2):159-68. PubMed ID: 6231138
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 33(6):907-15. PubMed ID: 6459736
    [TBL] [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; 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; 1885():233-250. PubMed ID: 30506202
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Fetal hexosaminidase A in mother's serum: pitfalls for carrier detection and prospects for prenatal diagnoses of GM2 gangliosidoses.
    Navon R; Lejbkowicz I; Adam A
    Am J Hum Genet; 1987 Jan; 40(1):60-1. PubMed ID: 2949607
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.