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 *

83 related articles for article (PubMed ID: 7943033)

  • 1. Unstable triplets and their mutational mechanism: size reduction of the CGG repeat vs. germline mosaicism in the fragile X syndrome.
    Chiurazzi P; Kozak L; Neri G
    Am J Med Genet; 1994 Jul; 51(4):517-21. PubMed ID: 7943033
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Fragile X syndrome: discordant levels of CGG repeat mosaicism in two brothers.
    Mueller OT; Hartsfield JK; Amar MJ; Gallardo LA; Kousseff BG
    Am J Med Genet; 1995 Aug; 60(4):302-6. PubMed ID: 7485265
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Unstable DNA sequence and methylation in fragile X syndrome].
    Fu SD; Shen Y; Fan Y
    Zhonghua Yi Xue Za Zhi; 1994 Oct; 74(10):611-4, 646-7. PubMed ID: 7842338
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. A point mutation in the FMR-1 gene associated with fragile X mental retardation.
    De Boulle K; Verkerk AJ; Reyniers E; Vits L; Hendrickx J; Van Roy B; Van den Bos F; de Graaff E; Oostra BA; Willems PJ
    Nat Genet; 1993 Jan; 3(1):31-5. PubMed ID: 8490650
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A complex mutable polymorphism located within the fragile X gene.
    Zhong N; Dobkin C; Brown WT
    Nat Genet; 1993 Nov; 5(3):248-53. PubMed ID: 8275089
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mosaicism in fragile X affected males.
    Nolin SL; Glicksman A; Houck GE; Brown WT; Dobkin CS
    Am J Med Genet; 1994 Jul; 51(4):509-12. PubMed ID: 7943031
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Evidence of founder chromosomes in fragile X syndrome.
    Richards RI; Holman K; Friend K; Kremer E; Hillen D; Staples A; Brown WT; Goonewardena P; Tarleton J; Schwartz C
    Nat Genet; 1992 Jul; 1(4):257-60. PubMed ID: 1302021
    [TBL] [Abstract][Full Text] [Related]  

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

  • 10. Germline mosaicism at the fragile X locus.
    Prior TW; Papp AC; Snyder PJ; Sedra MS; Guida M; Enrile BG
    Am J Med Genet; 1995 Jan; 55(3):384-6. PubMed ID: 7726241
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Monozygotic twin brothers with the fragile X syndrome: different CGG repeats and different mental capacities.
    Helderman-van den Enden AT; Maaswinkel-Mooij PD; Hoogendoorn E; Willemsen R; Maat-Kievit JA; Losekoot M; Oostra BA
    J Med Genet; 1999 Mar; 36(3):253-7. PubMed ID: 10204857
    [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. [Experimental therapy: reactivation of the FMR1 gene involved in fragile X syndrome].
    Chiurazzi P; Neri G
    Rev Neurol; 2001 Oct; 33 Suppl 1():S62-5. PubMed ID: 12447822
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Robust amplification and ethidium-visible detection of the fragile X syndrome CGG repeat using Pfu polymerase.
    Chong SS; Eichler EE; Nelson DL; Hughes MR
    Am J Med Genet; 1994 Jul; 51(4):522-6. PubMed ID: 7943034
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Molecular and genetic features of fragile X syndrome].
    Jara L; Avendaño I; Aspillaga M; Blanco R
    Rev Med Chil; 1996 Jul; 124(7):865-72. PubMed ID: 9138377
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. [A genetic and molecular study of 85 families affected with the fragile X syndrome].
    Milà Recasens M; Sánchez Díaz A; Glover López G; Castellví Bel S; Carbonell Meseguer P; Kruyer H; Ballesta Martínez F; Estivill Pallejà X
    An Esp Pediatr; 1996 Mar; 44(3):250-6. PubMed ID: 8830601
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Characterization and localization of the FMR-1 gene product associated with fragile X syndrome.
    Verheij C; Bakker CE; de Graaff E; Keulemans J; Willemsen R; Verkerk AJ; Galjaard H; Reuser AJ; Hoogeveen AT; Oostra BA
    Nature; 1993 Jun; 363(6431):722-4. PubMed ID: 8515814
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Analysis of CGG variation through 642 meioses in Fragile X families.
    Rifé M; Badenas C; Quintó L; Puigoriol E; Tazón B; Rodriguez-Revenga L; Jiménez L; Sánchez A; Milà M
    Mol Hum Reprod; 2004 Oct; 10(10):773-6. PubMed ID: 15322225
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.