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Journal Abstract Search

166 related items for PubMed ID: 3783617

  • 1. 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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  • 2. 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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  • 6. 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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  • 9. In situ nick translation of the fragile X region.
    Nolin SL, Jenkins EC, Brown WT, Dobkin CS.
    Am J Med Genet; 1988 Jul; 30(1-2):443-50. PubMed ID: 3052067
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  • 11. Replication patterns of the fragile X in heterozygous carriers: analysis by a BrdUrd antibody method.
    Ohashi H, Kuwano A, Tsukahara M, Arinami T, Kajii T.
    Am J Hum Genet; 1990 Dec; 47(6):988-93. PubMed ID: 2239973
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  • 12. Unusual X chromosome inactivation in a mentally retarded girl with an interstitial deletion Xq27: implications for the fragile X syndrome.
    Schmidt M, Certoma A, Du Sart D, Kalitsis P, Leversha M, Fowler K, Sheffield L, Jack I, Danks DM.
    Hum Genet; 1990 Mar; 84(4):347-52. PubMed ID: 2307456
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  • 13. Triradial configurations indicate that expression of the fragile site at Xq27 is non-lethal.
    Tommerup N.
    Ann Genet; 1987 Mar; 30(4):231-2. PubMed ID: 3501266
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  • 17. Fragile X syndrome: a hypothesis regarding the molecular mechanism of the phenotype.
    Warren ST.
    Am J Med Genet; 1988 Mar; 30(1-2):681-8. PubMed ID: 3177478
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  • 20. Increased sister chromatid exchange frequency at Xq27 site in affected fragile X males.
    Wenger SL, Hennessey JC, Steele MW.
    Am J Med Genet; 1987 Apr; 26(4):909-14. PubMed ID: 3591833
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