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Journal Abstract Search

128 related items for PubMed ID: 3177457

  • 1. Prenatal diagnosis of the fragile X--the Australasian experience.
    Purvis-Smith SG, Laing S, Sutherland GR, Baker E.
    Am J Med Genet; 1988; 30(1-2):337-45. PubMed ID: 3177457
    [Abstract] [Full Text] [Related]

  • 2. Experience with multiple approaches to the prenatal diagnosis of the fragile X syndrome: amniotic fluid, chorionic villi, fetal blood and molecular methods.
    Shapiro LR, Wilmot PL, Murphy PD, Breg WR.
    Am J Med Genet; 1988; 30(1-2):347-54. PubMed ID: 2902794
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  • 3. Recent experience in prenatal fra(X) detection.
    Jenkins EC, Brown WT, Krawczun MS, Duncan CJ, Lele KP, Cantu ES, Schonberg S, Golbus MS, Sekhon GS, Stark S.
    Am J Med Genet; 1988; 30(1-2):329-36. PubMed ID: 2972205
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  • 4. Prenatal diagnosis of fragile X syndrome by placental (chorionic villi) biopsy culture.
    McKinley MJ, Kearney LU, Nicolaides KH, Gosden CM, Webb TP, Fryns JP.
    Am J Med Genet; 1988; 30(1-2):355-68. PubMed ID: 3177458
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  • 5. The prenatal detection of the fragile X chromosome: review of recent experience.
    Jenkins EC, Brown WT, Wilson MG, Lin MS, Alfi OS, Wassman ER, Brooks J, Duncan CJ, Masia A, Krawczun MS.
    Am J Med Genet; 1986; 23(1-2):297-311. PubMed ID: 2937295
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  • 7. Prenatal diagnosis of the fragile X syndrome: possible end of the experimental phase for amniotic fluid.
    Shapiro LR, Wilmot PL, Murphy PD.
    Am J Med Genet; 1991; 38(2-3):453-5. PubMed ID: 1673318
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  • 9. Prenatal diagnosis of the fragile X using thymidine induction.
    Sutherland GR, Baker E, Purvis-Smith S, Hockey A, Krumins E, Eichenbaum SZ.
    Prenat Diagn; 1987 Mar; 7(3):197-202. PubMed ID: 2954037
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  • 10. Second trimester prenatal diagnosis of the fragile X.
    Tommerup N, Aula P, Gustavii B, Heiberg A, Holmgren G, von Koskull H, Leisti J, Mikkelsen M, Mitelman F, Nielsen KB.
    Am J Med Genet; 1986 Mar; 23(1-2):313-24. PubMed ID: 2937296
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  • 11. The use of early simultaneous percutaneous umbilical blood sampling (PUBS) and amniocentesis for prenatal fragile X chromosome diagnosis.
    Butler MG, Dev VG, Shah D, Ulm JE, Wilmot PL, Shapiro LR.
    Am J Med Genet; 1988 Dec; 31(4):775-8. PubMed ID: 3239566
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  • 13. Missed prenatal diagnosis of fragile-X syndrome.
    Webb TP, Bundey S, McKinley M.
    Prenat Diagn; 1989 Nov; 9(11):777-81. PubMed ID: 2616536
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  • 15. Differential expression of fragile site Xq27 in cultured fibroblasts from hemizygotes and heterozygotes and its implications for prenatal diagnosis.
    Schmidt A, Passarge E.
    Am J Med Genet; 1986 Nov; 23(1-2):515-25. PubMed ID: 3953662
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  • 16. Prenatal diagnosis of fragile X in a heterozygous female fetus and postnatal follow-up.
    Wilson MG, Marchese CA.
    Prenat Diagn; 1984 Nov; 4(1):61-6. PubMed ID: 6728827
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  • 18. Laboratory aspects of prenatal fra(X) detection.
    Jenkins EC, Krawczun MS, Brooks SE, Brooks SL, Sherman SL, Brown WT.
    Prog Clin Biol Res; 1991 Nov; 368():27-42. PubMed ID: 1835094
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  • 20. Cytogenetic experience in prenatal fra(X) detection on amniotic fluid cultures.
    Devillard F, Prieur F, Delhomme-Bachy M, De Freminville B, Lauras B, Brizard CP, Fraisse J, Bertheas MF.
    Prenat Diagn; 1992 Jul; 12(7):613-8. PubMed ID: 1508852
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