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143 related items for PubMed ID: 3953662

  • 1. 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; 23(1-2):515-25. PubMed ID: 3953662
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  • 2. Prenatal diagnosis of fragile (X) syndrome.
    Hogge WA, Schonberg SA, Glover TW, Hecht F, Golbus MS.
    Obstet Gynecol; 1984 Mar; 63(3 Suppl):19S-21S. PubMed ID: 6700875
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  • 3. [Prenatal diagnosis of a male fetal carrier of fragile X chromosome by the amniotic fluid cells].
    Tejada I, Boué J, Gilgenkrantz S.
    Ann Genet; 1983 Mar; 26(4):247-50. PubMed ID: 6607707
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  • 6. The fragile X(q27) form of X-linked mental retardation: FUdR as an inducing agent for fra(X)(q27) expression in lymphocytes, fibroblasts, and amniocytes.
    Brookwell R, Daniel A, Turner G, Fishburn J.
    Am J Med Genet; 1982 Oct; 13(2):139-48. PubMed ID: 6215863
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  • 7. 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 Oct; 30(1-2):355-68. PubMed ID: 3177458
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  • 8. 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 Oct; 30(1-2):329-36. PubMed ID: 2972205
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  • 11. Prenatal diagnosis of the fragile X--the Australasian experience.
    Purvis-Smith SG, Laing S, Sutherland GR, Baker E.
    Am J Med Genet; 1988 Oct; 30(1-2):337-45. PubMed ID: 3177457
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  • 12. Prenatal diagnosis of fragile X in a heterozygous female fetus and postnatal follow-up.
    Wilson MG, Marchese CA.
    Prenat Diagn; 1984 Oct; 4(1):61-6. PubMed ID: 6728827
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  • 13. Manifestation of the fragile site Xq27 in fibroblasts. III. A method to demonstrate R-type replication patterns and the fragile site.
    Barbi G, Steinbach P, Wiedenmann A, Vogel W.
    Hum Genet; 1983 Oct; 65(1):76-8. PubMed ID: 6642510
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  • 14. Expression of the fragile site Xq27 in fibroblasts. I. Detection of fra(X)(q27) in fibroblast clones from males with X-linked mental retardation.
    Steinbach P, Barbi G, Baur S, Wiedenmann A.
    Hum Genet; 1983 Oct; 63(4):404-5. PubMed ID: 6683244
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  • 15. Distribution of diploidy, polyploidy, and endoreduplication in fra(X) positive and negative lymphocytes, amniocytes, and chorionic villi.
    Jenkins EC, Sanz MM, Ray JH, Stark-Houck SL, Brown WT.
    Am J Med Genet; 1991 Oct; 38(2-3):434-6. PubMed ID: 1826811
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  • 16. Prenatal diagnosis of X-linked mental retardation with fragile (X) using fetoscopy and fetal blood sampling.
    Webb T, Gosden CM, Rodeck CH, Hamill MA, Eason PE.
    Prenat Diagn; 1983 Oct; 3(2):131-7. PubMed ID: 6622392
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  • 18. On the frequency of telomeric chromosomal changes induced by culture conditions suitable for fragile X expression.
    Steinbach P, Barbi G, Böller T.
    Hum Genet; 1982 Oct; 61(2):160-2. PubMed ID: 7129442
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  • 20. Fragile X expression in normal and mentally retarded subjects: effect of treatment with an antifolic agent.
    Sanfilippo S, Ragusa RM, Scillato F, Ruggeri M, Neri G.
    Am J Med Genet; 1988 Oct; 30(1-2):369-76. PubMed ID: 3177459
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