BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

121 related articles for article (PubMed ID: 7726212)

  • 1. Neurobehavioral characteristics of CGG amplification status in fragile X females.
    Thompson NM; Gulley ML; Rogeness GA; Clayton RJ; Johnson C; Hazelton B; Cho CG; Zellmer VT
    Am J Med Genet; 1994 Dec; 54(4):378-83. PubMed ID: 7726212
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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; 42(14):1934-47. PubMed ID: 15381024
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Neuropsychological profiles of three sisters homozygous for the fragile X premutation.
    Mazzocco MM; Holden JJ
    Am J Med Genet; 1996 Aug; 64(2):323-8. PubMed ID: 8844074
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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; 57(1):53-60. PubMed ID: 15629215
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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; 64(2):340-5. PubMed ID: 8844077
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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; 64(2):329-33. PubMed ID: 8844075
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Contribution of the FMR1 gene mutation to human intellectual dysfunction.
    Reiss AL; Freund LS; Baumgardner TL; Abrams MT; Denckla MB
    Nat Genet; 1995 Nov; 11(3):331-4. PubMed ID: 7581460
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Neurobehavioral phenotype in carriers of the fragile X premutation.
    Johnston C; Eliez S; Dyer-Friedman J; Hessl D; Glaser B; Blasey C; Taylor A; Reiss A
    Am J Med Genet; 2001 Nov; 103(4):314-9. PubMed ID: 11746012
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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; 271(7):507-14. PubMed ID: 8301764
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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; 127(Pt 12):2672-81. PubMed ID: 15483045
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Molecular-intelligence correlations in young fragile X males with a mild CGG repeat expansion in the FMR1 gene.
    Steyaert J; Borghgraef M; Legius E; Fryns JP
    Am J Med Genet; 1996 Aug; 64(2):274-7. PubMed ID: 8844064
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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; 5(4):377-80. PubMed ID: 7888141
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A methylation PCR approach for detection of fragile X syndrome.
    Panagopoulos I; Lassen C; Kristoffersson U; Aman P
    Hum Mutat; 1999; 14(1):71-9. PubMed ID: 10447261
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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; 64(2):388-94. PubMed ID: 8844089
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mosaicism in a fragile X male including a de novo deletion in the FMR1 gene.
    Petek E; Kroisel PM; Schuster M; Zierler H; Wagner K
    Am J Med Genet; 1999 May; 84(3):229-32. PubMed ID: 10331598
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Fragile X syndrome and deletions in FMR1: new case and review of the literature.
    Hammond LS; Macias MM; Tarleton JC; Shashidhar Pai G
    Am J Med Genet; 1997 Nov; 72(4):430-4. PubMed ID: 9375726
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The full mutation in the FMR-1 gene of male fragile X patients is absent in their sperm.
    Reyniers E; Vits L; De Boulle K; Van Roy B; Van Velzen D; de Graaff E; Verkerk AJ; Jorens HZ; Darby JK; Oostra B
    Nat Genet; 1993 Jun; 4(2):143-6. PubMed ID: 8348152
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A fragile gene.
    Oostra BA; Willems PJ
    Bioessays; 1995 Nov; 17(11):941-7. PubMed ID: 8526888
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Deletion in the FMR1 gene in a fragile-X male.
    Mannermaa A; Pulkkinen L; Kajanoja E; Ryynänen M; Saarikoski S
    Am J Med Genet; 1996 Aug; 64(2):293-5. PubMed ID: 8844068
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Emotional and neurocognitive deficits in fragile X.
    Sobesky WE; Pennington BF; Porter D; Hull CE; Hagerman RJ
    Am J Med Genet; 1994 Jul; 51(4):378-85. PubMed ID: 7943003
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.