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 *

177 related articles for article (PubMed ID: 7842338)

  • 1. [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]  

  • 2. 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]  

  • 3. 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]  

  • 4. [Detection of FMR-1 gene expression by RT-PCR].
    Zheng L; Fan Y; Huang T; Zhu N; Shen Y; Wu G
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1995 Dec; 17(6):407-11. PubMed ID: 9208564
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [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]  

  • 6. 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]  

  • 7. Relationship of expansion of CGG repeats and X-inactivation with expression of fra(X)(q27.3) in heterozygotes.
    Mingroni-Netto RC; Fernandes JG; Vianna-Morgante AM
    Am J Med Genet; 1994 Jul; 51(4):443-6. PubMed ID: 7943014
    [TBL] [Abstract][Full Text] [Related]  

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

  • 9. 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]  

  • 10. 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]  

  • 11. [Pathology of unstable sequence of genome: fragile-X-syndrome].
    Beldjord C; Richard L
    C R Seances Soc Biol Fil; 1992; 186(4):363-70. PubMed ID: 1301224
    [TBL] [Abstract][Full Text] [Related]  

  • 12. DNA diagnosis of the fragile X syndrome in a series of 236 mentally retarded subjects and evidence for a reversal of mutation in the FMR-1 gene.
    van den Ouweland AM; de Vries BB; Bakker PL; Deelen WH; de Graaff E; van Hemel JO; Oostra BA; Niermeijer MF; Halley DJ
    Am J Med Genet; 1994 Jul; 51(4):482-5. PubMed ID: 7943024
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular characterization of the fragile-X syndrome in the Mexican population.
    Díaz-Gallardo MY; Barros-Núñez P; Díaz CA; Hernández A; Gómez-Espinel I; Leal CA; Fragoso R; Figuera L; García-Cruz D; Ramírez-Dueñas ML
    Arch Med Res; 1995; 26 Spec No():S77-83. PubMed ID: 8845662
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Molecular pathology of the fragile X syndrome.
    Tsongalis GJ; Silverman LM
    Arch Pathol Lab Med; 1993 Nov; 117(11):1121-5. PubMed ID: 8239933
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Prediction of mental status in carriers of the fragile X mutation using CGG repeat length.
    Smits A; Smeets D; Hamel B; Dreesen J; de Haan A; van Oost B
    Am J Med Genet; 1994 Jul; 51(4):497-500. PubMed ID: 7943027
    [TBL] [Abstract][Full Text] [Related]  

  • 16. In vitro DNA methylation inhibits FMR-1 promoter.
    Hwu WL; Lee YM; Lee SC; Wang TR
    Biochem Biophys Res Commun; 1993 May; 193(1):324-9. PubMed ID: 8503923
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. The FMR-1 protein is cytoplasmic, most abundant in neurons and appears normal in carriers of a fragile X premutation.
    Devys D; Lutz Y; Rouyer N; Bellocq JP; Mandel JL
    Nat Genet; 1993 Aug; 4(4):335-40. PubMed ID: 8401578
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [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]  

  • 20. Isolation of a GCC repeat showing expansion in FRAXF, a fragile site distal to FRAXA and FRAXE.
    Parrish JE; Oostra BA; Verkerk AJ; Richards CS; Reynolds J; Spikes AS; Shaffer LG; Nelson DL
    Nat Genet; 1994 Nov; 8(3):229-35. PubMed ID: 7874164
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.