These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

191 related articles for article (PubMed ID: 7943005)

  • 1. Transmitting males and carrier females in fragile X--revisited.
    Loesch DZ; Hay DA; Mulley J
    Am J Med Genet; 1994 Jul; 51(4):392-9. PubMed ID: 7943005
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. High functioning fragile X males: demonstration of an unmethylated fully expanded FMR-1 mutation associated with protein expression.
    Hagerman RJ; Hull CE; Safanda JF; Carpenter I; Staley LW; O'Connor RA; Seydel C; Mazzocco MM; Snow K; Thibodeau SN
    Am J Med Genet; 1994 Jul; 51(4):298-308. PubMed ID: 7942991
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [New methods for the diagnosis of fragile X syndrome: a study of the FMRP in blood and hair].
    Ramos-Fuentes FJ
    Rev Neurol; 2001 Oct; 33 Suppl 1():S9-S13. PubMed ID: 12447812
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Expansion mutation frequency and CGG/GCC repeat polymorphism in FMR1 and FMR2 genes in an Indian population.
    Sharma D; Gupta M; Thelma BK
    Genet Epidemiol; 2001 Jan; 20(1):129-144. PubMed ID: 11119302
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. FMRP expression as a potential prognostic indicator in fragile X syndrome.
    Tassone F; Hagerman RJ; Iklé DN; Dyer PN; Lampe M; Willemsen R; Oostra BA; Taylor AK
    Am J Med Genet; 1999 May; 84(3):250-61. PubMed ID: 10331602
    [TBL] [Abstract][Full Text] [Related]  

  • 10. No apparent involvement of the FMR1 gene in five patients with phenotypic manifestations of the fragile X syndrome.
    Chiurazzi P; de Graaff E; Ng J; Verkerk AJ; Wolfson S; Fisch GS; Kozak L; Neri G; Oostra BA
    Am J Med Genet; 1994 Jul; 51(4):309-14. PubMed ID: 7942992
    [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. Fragile X mental retardation syndrome: from pathogenesis to diagnostic issues.
    Mandel JL; Biancalana V
    Growth Horm IGF Res; 2004 Jun; 14 Suppl A():S158-65. PubMed ID: 15135801
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Fragile X syndrome without CCG amplification has an FMR1 deletion.
    Gedeon AK; Baker E; Robinson H; Partington MW; Gross B; Manca A; Korn B; Poustka A; Yu S; Sutherland GR
    Nat Genet; 1992 Aug; 1(5):341-4. PubMed ID: 1302032
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Molecular analysis of the fragile X syndrome.
    Knight SJ; Hirst MC; Davies KE
    Dis Markers; 1992; 10(1):1-5. PubMed ID: 1424438
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. The fragile X phenotype in a mosaic male with a deletion showing expression of the FMR1 protein in 28% of the cells.
    de Graaff E; de Vries BB; Willemsen R; van Hemel JO; Mohkamsing S; Oostra BA; van den Ouweland AM
    Am J Med Genet; 1996 Aug; 64(2):302-8. PubMed ID: 8844070
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genotype, molecular phenotype, and cognitive phenotype: correlations in fragile X syndrome.
    Kaufmann WE; Abrams MT; Chen W; Reiss AL
    Am J Med Genet; 1999 Apr; 83(4):286-95. PubMed ID: 10208163
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Fragile X syndrome.
    Laxova R
    Adv Pediatr; 1994; 41():305-42. PubMed ID: 7992687
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 10.