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Journal Abstract Search

971 related items for PubMed ID: 8301764

  • 1. Molecular predictors of cognitive involvement in female carriers of fragile X syndrome.
    Taylor AK, Safanda JF, Fall MZ, Quince C, Lang KA, Hull CE, Carpenter I, Staley LW, Hagerman RJ.
    JAMA; 1994 Feb 16; 271(7):507-14. PubMed ID: 8301764
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  • 2. Advances in molecular analysis of fragile X syndrome.
    Warren ST, Nelson DL.
    JAMA; 1994 Feb 16; 271(7):536-42. PubMed ID: 8301769
    [Abstract] [Full Text] [Related]

  • 3. The emerging fragile X premutation phenotype: evidence from the domain of social cognition.
    Cornish K, Kogan C, Turk J, Manly T, James N, Mills A, Dalton A.
    Brain Cogn; 2005 Feb 16; 57(1):53-60. PubMed ID: 15629215
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  • 4. Tissue-specific methylation differences and cognitive function in fragile X premutation females.
    Allingham-Hawkins DJ, Brown CA, Babul R, Chitayat D, Krekewich K, Humphries T, Ray PN, Teshima IE.
    Am J Med Genet; 1996 Aug 09; 64(2):329-33. PubMed ID: 8844075
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  • 5. The effect of pre-mutation of X chromosome CGG trinucleotide repeats on brain anatomy.
    Moore CJ, Daly EM, Tassone F, Tysoe C, Schmitz N, Ng V, Chitnis X, McGuire P, Suckling J, Davies KE, Hagerman RJ, Hagerman PJ, Murphy KC, Murphy DG.
    Brain; 2004 Dec 09; 127(Pt 12):2672-81. PubMed ID: 15483045
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  • 6. Molecular-clinical correlations in males with an expanded FMR1 mutation.
    Merenstein SA, Sobesky WE, Taylor AK, Riddle JE, Tran HX, Hagerman RJ.
    Am J Med Genet; 1996 Aug 09; 64(2):388-94. PubMed ID: 8844089
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  • 7. A neuropsychological investigation of male premutation carriers of fragile X syndrome.
    Moore CJ, Daly EM, Schmitz N, Tassone F, Tysoe C, Hagerman RJ, Hagerman PJ, Morris RG, Murphy KC, Murphy DG.
    Neuropsychologia; 2004 Aug 09; 42(14):1934-47. PubMed ID: 15381024
    [Abstract] [Full Text] [Related]

  • 8. Molecular/clinical correlations in females with fragile X.
    Sobesky WE, Taylor AK, Pennington BF, Bennetto L, Porter D, Riddle J, Hagerman RJ.
    Am J Med Genet; 1996 Aug 09; 64(2):340-5. PubMed ID: 8844077
    [Abstract] [Full Text] [Related]

  • 9. A deletion of 1.6 Kb proximal to the CGG repeat of the FMR1 gene causes fragile X-like psychological features.
    Wiegers AM, Curfs LM, Meijer H, Oostra B, Fryns JP.
    Genet Couns; 1994 Aug 09; 5(4):377-80. PubMed ID: 7888141
    [Abstract] [Full Text] [Related]

  • 10. The risk of fragile X premutation expansion is lower in carriers detected by general prenatal screening than in carriers from known fragile X families.
    Geva E, Yaron Y, Shomrat R, Ben-Yehuda A, Zabari S, Peretz H, Naiman T, Yeger H, Orr-Urtreger A.
    Genet Test; 2000 Aug 09; 4(3):289-92. PubMed ID: 11142761
    [Abstract] [Full Text] [Related]

  • 11. Apparent regression of the CGG repeat in FMR1 to an allele of normal size.
    Vits L, De Boulle K, Reyniers E, Handig I, Darby JK, Oostra B, Willems PJ.
    Hum Genet; 1994 Nov 09; 94(5):523-6. PubMed ID: 7959688
    [Abstract] [Full Text] [Related]

  • 12. Methylation mosaicism of 5'-(CGG)(n)-3' repeats in fragile X, premutation and normal individuals.
    Genç B, Müller-Hartmann H, Zeschnigk M, Deissler H, Schmitz B, Majewski F, von Gontard A, Doerfler W.
    Nucleic Acids Res; 2000 May 15; 28(10):2141-52. PubMed ID: 10773084
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  • 14. A female compound heterozygote (pre- and full mutation) for the CGG FMR1 expansion.
    Milà M, Castellví-Bel S, Giné R, Vazquez C, Badenas C, Sánchez A, Estivill X.
    Hum Genet; 1996 Oct 15; 98(4):419-21. PubMed ID: 8792815
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  • 18. FMR1 gene deletion/reversion: a pitfall of fragile X carrier testing.
    Gasteiger M, Grasbon-Frodl E, Neitzel B, Kooy F, Holinski-Feder E.
    Genet Test; 2003 Oct 15; 7(4):303-8. PubMed ID: 15000806
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  • 19. Contribution of the FMR1 gene mutation to human intellectual dysfunction.
    Reiss AL, Freund LS, Baumgardner TL, Abrams MT, Denckla MB.
    Nat Genet; 1995 Nov 15; 11(3):331-4. PubMed ID: 7581460
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