BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

142 related articles for article (PubMed ID: 9456366)

  • 1. [Analysis of expression of FMR-1 gene in male patients with fragile X syndrome using RT-PCR].
    Zhu W; Li M; Zhao Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1998 Feb; 15(1):17-9. PubMed ID: 9456366
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [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]  

  • 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. 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]  

  • 5. Novel point mutation within intron 10 of FMR-1 gene causing fragile X syndrome.
    Wang YC; Lin ML; Lin SJ; Li YC; Li SY
    Hum Mutat; 1997; 10(5):393-9. PubMed ID: 9375856
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Tissue specific expression of FMR-1 provides evidence for a functional role in fragile X syndrome.
    Hinds HL; Ashley CT; Sutcliffe JS; Nelson DL; Warren ST; Housman DE; Schalling M
    Nat Genet; 1993 Jan; 3(1):36-43. PubMed ID: 8490651
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Non-invasive screening of fragile X syndrome A using urine and hair roots.
    Suwa K; Momoi MY
    Brain Dev; 2004 Sep; 26(6):380-3. PubMed ID: 15275700
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Direct molecular analysis of FMR-1 gene mutation in patients with fragile Xq syndrome and their families].
    Alliende MA; Urzúa B; Valiente A; Cortés F; Curotto B; Rojas C
    Rev Med Chil; 1998 Dec; 126(12):1435-46. PubMed ID: 10349157
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Pilot study for the neonatal screening of fragile X syndrome.
    Rifé M; Mallolas J; Badenas C; Tazón B; Miguélez MR; Pàmpols T; Sànchez A; Milà M
    Prenat Diagn; 2002 Jun; 22(6):459-62. PubMed ID: 12116303
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Macrocephaly, hypospadias grade III-IV, and fragile X-like behavior in identical twins without involvement of the FMR-1 gene.
    Fryns JP; D'Hooghe M; Devriendt K
    Genet Couns; 1996; 7(3):227-30. PubMed ID: 8897045
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Preimplantation diagnosis for fragile X syndrome based on the detection of the non-expanded paternal and maternal CGG.
    Sermon K; Seneca S; Vanderfaeillie A; Lissens W; Joris H; Vandervorst M; Van Steirteghem A; Liebaers I
    Prenat Diagn; 1999 Dec; 19(13):1223-30. PubMed ID: 10660959
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Age dependent and tissue specific FMR-1 gene expression in human organs].
    Ito M; Sugie H
    Nihon Rinsho; 1999 Apr; 57(4):950-4. PubMed ID: 10222795
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Fragile X syndrome a case report of a family.
    Chatterjee C; Guha D; Das S; Singh SK; Dasgupta U; Saha S; Bannerjee D
    Indian J Pathol Microbiol; 2001 Oct; 44(4):499-502. PubMed ID: 12035381
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The fragile-X syndrome after the discovery of the FMR-1 gene. The clinical geneticist faced with the unravelled enigmas and persisting difficulties in genetic counseling.
    Fryns JP; Curfs LM; Cassiman JJ; van den Berghe H
    Genet Couns; 1992; 3(4):175-7. PubMed ID: 1361752
    [No Abstract]   [Full Text] [Related]  

  • 18. 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]  

  • 19. Molecular diagnosis and genetic counseling for fragile X mental retardation.
    Pandey UB; Phadke SR; Mittal B
    Neurol India; 2004 Mar; 52(1):36-42. PubMed ID: 15069237
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Diagnosis of Fragile X syndrome by Southern blot hybridization using a chemiluminescent probe: a laboratory protocol.
    Gold B; Radu D; Balanko A; Chiang CS
    Mol Diagn; 2000 Sep; 5(3):169-78. PubMed ID: 11070151
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.