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 *

130 related articles for article (PubMed ID: 7605796)

  • 1. The fragile X syndrome.
    Flannery AV; Hirst MC; Knight SJ; Ritchie RJ; Davies KE
    Biochim Biophys Acta; 1995 Jun; 1271(2-3):293-303. PubMed ID: 7605796
    [No Abstract]   [Full Text] [Related]  

  • 2. Alternative splicing in the fragile X gene FMR1.
    Verkerk AJ; de Graaff E; De Boulle K; Eichler EE; Konecki DS; Reyniers E; Manca A; Poustka A; Willems PJ; Nelson DL
    Hum Mol Genet; 1993 Aug; 2(8):1348. PubMed ID: 8401531
    [No Abstract]   [Full Text] [Related]  

  • 3. 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]  

  • 4. Instability of the CGG repeat at the FRAXA locus and variable phenotypic expression in a large fragile X pedigree.
    Pintado E; de Diego Y; Hmadcha A; Carrasco M; Sierra J; Lucas M
    J Med Genet; 1995 Nov; 32(11):907-8. PubMed ID: 8592340
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Fragile X syndrome: (What's) lost in translation?
    Miyashiro K; Eberwine J
    Proc Natl Acad Sci U S A; 2004 Dec; 101(50):17329-30. PubMed ID: 15583122
    [No Abstract]   [Full Text] [Related]  

  • 6. KH domains within the FMR1 sequence suggest that fragile X syndrome stems from a defect in RNA metabolism.
    Gibson TJ; Rice PM; Thompson JD; Heringa J
    Trends Biochem Sci; 1993 Sep; 18(9):331-3. PubMed ID: 7694397
    [No Abstract]   [Full Text] [Related]  

  • 7. The fragile X syndrome: isolation of the FMR-1 gene and characterization of the fragile X mutation.
    Oostra BA; Verkerk AJ
    Chromosoma; 1992 Apr; 101(7):381-7. PubMed ID: 1618021
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Distribution of CGG repeat sizes within the fragile X mental retardation 1 (FMR1) homologue in a non-human primate population.
    Garcia Arocena D; Breece KE; Hagerman PJ
    Hum Genet; 2003 Oct; 113(5):371-6. PubMed ID: 12905066
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. X inactivation of the FMR1 fragile X mental retardation gene.
    Kirchgessner CU; Warren ST; Willard HF
    J Med Genet; 1995 Dec; 32(12):925-9. PubMed ID: 8825916
    [TBL] [Abstract][Full Text] [Related]  

  • 11. New insights into fragile X syndrome: from molecules to neurobehaviors.
    Jin P; Warren ST
    Trends Biochem Sci; 2003 Mar; 28(3):152-8. PubMed ID: 12633995
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Fmr1 knockout mice: a model to study fragile X mental retardation. The Dutch-Belgian Fragile X Consortium.
    Cell; 1994 Jul; 78(1):23-33. PubMed ID: 8033209
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Clinical and genetic aspects of fragile X mental retardation syndrome].
    Islamgulov DV; Karunas AS; Valinurov RG; Khusnutdinova EK
    Zh Nevrol Psikhiatr Im S S Korsakova; 2005; 105(8):69-74. PubMed ID: 16180508
    [No Abstract]   [Full Text] [Related]  

  • 14. Methylation analysis of CGG sites in the CpG island of the human FMR1 gene.
    Hansen RS; Gartler SM; Scott CR; Chen SH; Laird CD
    Hum Mol Genet; 1992 Nov; 1(8):571-8. PubMed ID: 1301165
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Fine structure of the human FMR1 gene.
    Eichler EE; Richards S; Gibbs RA; Nelson DL
    Hum Mol Genet; 1994 Apr; 3(4):684-5. PubMed ID: 8069329
    [No Abstract]   [Full Text] [Related]  

  • 16. FMRP expression studies in blood and hair roots in a fragile X family with methylation mosaics.
    de Vries BB; Severijnen LA; Jacobs A; Olmer R; Halley DJ; Oostra BA; Willemsen R
    J Med Genet; 2003 Jul; 40(7):535-9. PubMed ID: 12843328
    [No Abstract]   [Full Text] [Related]  

  • 17. Spontaneous deletion in the FMR1 gene in a patient with fragile X syndrome and cherubism.
    Quan F; Grompe M; Jakobs P; Popovich BW
    Hum Mol Genet; 1995 Sep; 4(9):1681-4. PubMed ID: 8541863
    [No Abstract]   [Full Text] [Related]  

  • 18. Comment: How many are too many when discussing triplet repeats in the FMR1 gene and the Fragile X syndrome?
    Gilbert F
    Genet Test; 2001; 5(2):139-40. PubMed ID: 11551101
    [No Abstract]   [Full Text] [Related]  

  • 19. Compound heterozygous female with fragile X syndrome.
    Linden MG; Tassone F; Gane LW; Hills JL; Hagerman RJ; Taylor AK
    Am J Med Genet; 1999 Apr; 83(4):318-21. PubMed ID: 10208169
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The female and the fragile X reviewed.
    Kenneson A; Warren ST
    Semin Reprod Med; 2001 Jun; 19(2):159-65. PubMed ID: 11480913
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.