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Journal Abstract Search

217 related items for PubMed ID: 2766560

  • 1. The inactivation of the fragile X chromosome in female carriers of the Martin Bell syndrome as studied by two different methods.
    Tuckerman E, Webb T.
    Clin Genet; 1989 Jul; 36(1):25-30. PubMed ID: 2766560
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  • 2. Effect of X inactivation on fragile X frequency and mental retardation.
    Rosenberg C, Vianna-Morgante AM, Otto PA, Navajas L.
    Am J Med Genet; 1991 Jul; 38(2-3):421-4. PubMed ID: 2018084
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  • 3. Mental retardation in heterozygotes for the fragile-X mutation: evidence in favor of an X inactivation-dependent effect.
    Rocchi M, Archidiacono N, Rinaldi A, Filippi G, Bartolucci G, Fancello GS, Siniscalco M.
    Am J Hum Genet; 1990 Apr; 46(4):738-43. PubMed ID: 2316520
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  • 4. Fragile Xq27.3 in female heterozygotes for the Martin-Bell syndrome.
    Webb T, Jacobs PA.
    J Med Genet; 1990 Oct; 27(10):627-31. PubMed ID: 2246771
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  • 8. Frequency and replication status of the fragile X, fra(X)(q27-28), in a pair of monozygotic twins of markedly differing intelligence.
    Tuckerman E, Webb T, Bundey SE.
    J Med Genet; 1985 Apr; 22(2):85-91. PubMed ID: 4039370
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  • 9. Autism in fragile X females.
    Hagerman RJ, Chudley AE, Knoll JH, Jackson AW, Kemper M, Ahmad R.
    Am J Med Genet; 1986 Apr; 23(1-2):375-80. PubMed ID: 3953655
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  • 10. Expression of the fragile site Xq27 in fibroblasts. II. Evidence for negative and positive clones from heterozygous females and possible relationship between frequency and phenotype.
    Steinbach P, Barbi G, Baur S, Vogel W.
    Hum Genet; 1983 Apr; 64(3):279-82. PubMed ID: 6885072
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  • 12. Fra(X) frequency on the active X-chromosome and phenotype in heterozygous carriers of the fra(X) form of mental retardation.
    Wilhelm D, Froster-Iskenius U, Paul J, Schwinger E.
    Am J Med Genet; 1988 Apr; 30(1-2):407-15. PubMed ID: 3177461
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  • 13. Replication status of fragile X(q27.3) in 13 female heterozygotes.
    Tuckerman E, Webb T, Thake A.
    J Med Genet; 1986 Oct; 23(5):407-10. PubMed ID: 3783617
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  • 14. Fragile (X) X-linked mental retardation. II. Frequency and replication pattern of fragile (X)(q28) in heterozygotes.
    Knoll JH, Chudley AE, Gerrard JW.
    Am J Hum Genet; 1984 May; 36(3):640-5. PubMed ID: 6731439
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  • 15. X chromosome inactivation in fibroblasts of mentally retarded female carriers of the fragile site Xq27.3: application of the probe M27 beta to evaluate X inactivation status.
    Schmidt M, Du Sart D, Kalitsis P, Fraser N, Leversha M, Voullaire L, Foster D, Davies J, Hills L, Petrovic V.
    Am J Med Genet; 1991 May; 38(2-3):411-5. PubMed ID: 1673316
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  • 17. Fragile X chromosome: clinical and cytogenetic studies on cases from seven families.
    McDermott A, Walters R, Howell RT, Gardner A.
    J Med Genet; 1983 Jun; 20(3):169-78. PubMed ID: 6876108
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  • 18. Normal male carriers in the fra(X) form of X-linked mental retardation (Martin-Bell syndrome).
    Froster-Iskenius U, McGillivray BC, Dill FJ, Hall JG, Herbst DS.
    Am J Med Genet; 1986 Jun; 23(1-2):619-31. PubMed ID: 3953672
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  • 19. Replication status of the fragile X chromosome, fra(X)(q27), in three heterozygous females.
    Howell RT, McDermott A.
    Hum Genet; 1982 Jun; 62(3):282-4. PubMed ID: 7169220
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  • 20. Is there a fragile(X) negative Martin-Bell syndrome?
    Thode A, Laing S, Partington MW, Turner G.
    Am J Med Genet; 1988 Jun; 30(1-2):459-71. PubMed ID: 3052069
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