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 *

104 related articles for article (PubMed ID: 9799094)

  • 1. Polymorphism in the FMR1 gene.
    Gunter C; Warren ST
    Hum Genet; 1998 Sep; 103(3):365-6. PubMed ID: 9799094
    [No Abstract]   [Full Text] [Related]  

  • 2. Novel polymorphism in the FMR1 gene resulting in a "pseudodeletion" of FMR1 in a commonly used fragile X assay.
    Daly TM; Rafii A; Martin RA; Zehnbauer BA
    J Mol Diagn; 2000 Aug; 2(3):128-31. PubMed ID: 11229516
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Screening for FMR1 mutations among the mentally retarded: prevalence of the fragile X syndrome in Spain.
    Millán JM; Martínez F; Cadroy A; Gandía J; Casquero M; Beneyto M; Badía L; Prieto F
    Clin Genet; 1999 Jul; 56(1):98-9. PubMed ID: 10466426
    [No Abstract]   [Full Text] [Related]  

  • 4. FRAXAC1 and DXS548 polymorphisms in the Chinese population.
    Poon PM; Pang CP; Chen QL; Zhong N; Lai KY; Lau CH; Wong CK; Brown WT
    Am J Med Genet; 1999 May; 84(3):208-13. PubMed ID: 10331593
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Triplet repeat polymorphism & fragile X syndrome in the Indian context.
    Baskaran S; Naseerullah MK; Manjunatha KR; Chetan GK; Arthi R; Rao GV; Girimaji SR; Srinath S; Sheshadri S; Devi RR; Brahmachari V
    Indian J Med Res; 1998 Jan; 107():29-36. PubMed ID: 9529778
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Premutations in the FMR1 gene as a modifying factor in Parkin-associated Parkinson's disease?
    Hedrich K; Pramstaller PP; Stübke K; Hiller A; Kabakci K; Purmann S; Kasten M; Scaglione C; Schwinger E; Volkmann J; Kostic V; Vieregge P; Martinelli P; Abbruzzese G; Klein C; Zühlke C
    Mov Disord; 2005 Aug; 20(8):1060-2. PubMed ID: 15929093
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Haplotype analysis of the fragile X syndrome gene FMR1 in the Czech Republic.
    Pekarík V; Blazková M; Kozák L
    Am J Med Genet; 1999 May; 84(3):214-6. PubMed ID: 10331594
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Re-examination of factors associated with expansion of CGG repeats using a single nucleotide polymorphism in FMR1.
    Gunter C; Paradee W; Crawford DC; Meadows KA; Newman J; Kunst CB; Nelson DL; Schwartz C; Murray A; Macpherson JN; Sherman SL; Warren ST
    Hum Mol Genet; 1998 Nov; 7(12):1935-46. PubMed ID: 9811938
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Epigenetic variation illustrated by DNA methylation patterns of the fragile-X gene FMR1.
    Stöger R; Kajimura TM; Brown WT; Laird CD
    Hum Mol Genet; 1997 Oct; 6(11):1791-801. PubMed ID: 9302255
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The protein product of the fragile X gene, FMR1, has characteristics of an RNA-binding protein.
    Siomi H; Siomi MC; Nussbaum RL; Dreyfuss G
    Cell; 1993 Jul; 74(2):291-8. PubMed ID: 7688265
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. A deletion of 1.6 kb proximal to the CGG repeat of the FMR1 gene causes the clinical phenotype of the fragile X syndrome.
    Meijer H; de Graaff E; Merckx DM; Jongbloed RJ; de Die-Smulders CE; Engelen JJ; Fryns JP; Curfs PM; Oostra BA
    Hum Mol Genet; 1994 Apr; 3(4):615-20. PubMed ID: 8069307
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Transcription of the FMR1 gene in individuals with fragile X syndrome.
    Tassone F; Hagerman RJ; Chamberlain WD; Hagerman PJ
    Am J Med Genet; 2000; 97(3):195-203. PubMed ID: 11449488
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. 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]  

  • 19. Analysis of unstable DNA sequence in FMR1 gene in Polish families with fragile X syndrome.
    Milewski M; Zygulska M; Bal J; Deelen WH; Obersztyn E; Bocian E; Halley DJ; Horst J; Mazurczak T
    Acta Biochim Pol; 1996; 43(2):383-8. PubMed ID: 8862184
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Single-strand conformation polymorphism analysis in the FMR1 gene.
    Castellví-Bel S; Sánchez A; Badenas C; Mallolas J; Barceló A; Jiménez D; Villa M; Estivill X; Milà M
    Am J Med Genet; 1999 May; 84(3):262-5. PubMed ID: 10331603
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.