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 *

314 related articles for article (PubMed ID: 7833909)

  • 1. Sequence analysis of the fragile X trinucleotide repeat: implications for the origin of the fragile X mutation.
    Snow K; Tester DJ; Kruckeberg KE; Schaid DJ; Thibodeau SN
    Hum Mol Genet; 1994 Sep; 3(9):1543-51. PubMed ID: 7833909
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Haplotype and interspersion analysis of the FMR1 CGG repeat identifies two different mutational pathways for the origin of the fragile X syndrome.
    Eichler EE; Macpherson JN; Murray A; Jacobs PA; Chakravarti A; Nelson DL
    Hum Mol Genet; 1996 Mar; 5(3):319-30. PubMed ID: 8852655
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Haplotype and AGG-interspersion analysis of FMR1 (CGG)(n) alleles in the Danish population: implications for multiple mutational pathways towards fragile X alleles.
    Larsen LA; Armstrong JS; Grønskov K; Hjalgrim H; Macpherson JN; Brøndum-Nielsen K; Hasholt L; Nørgaard-Pedersen B; Vuust J
    Am J Med Genet; 2000 Jul; 93(2):99-106. PubMed ID: 10869110
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Length of uninterrupted CGG repeats determines instability in the FMR1 gene.
    Eichler EE; Holden JJ; Popovich BW; Reiss AL; Snow K; Thibodeau SN; Richards CS; Ward PA; Nelson DL
    Nat Genet; 1994 Sep; 8(1):88-94. PubMed ID: 7987398
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox.
    Fu YH; Kuhl DP; Pizzuti A; Pieretti M; Sutcliffe JS; Richards S; Verkerk AJ; Holden JJ; Fenwick RG; Warren ST
    Cell; 1991 Dec; 67(6):1047-58. PubMed ID: 1760838
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Population survey of the human FMR1 CGG repeat substructure suggests biased polarity for the loss of AGG interruptions.
    Eichler EE; Hammond HA; Macpherson JN; Ward PA; Nelson DL
    Hum Mol Genet; 1995 Dec; 4(12):2199-208. PubMed ID: 8634688
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Fragile X gene instability: anchoring AGGs and linked microsatellites.
    Zhong N; Yang W; Dobkin C; Brown WT
    Am J Hum Genet; 1995 Aug; 57(2):351-61. PubMed ID: 7668261
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Data on the CGG repeat at the fragile X site in the non-retarded Japanese population and family suggest the presence of a subgroup of normal alleles predisposing to mutate.
    Arinami T; Asano M; Kobayashi K; Yanagi H; Hamaguchi H
    Hum Genet; 1993 Nov; 92(5):431-6. PubMed ID: 8244331
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Precursor arrays for triplet repeat expansion at the fragile X locus.
    Hirst MC; Grewal PK; Davies KE
    Hum Mol Genet; 1994 Sep; 3(9):1553-60. PubMed ID: 7833910
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Analysis of a CGG sequence at the FMR-1 locus in fragile X families and in the general population.
    Snow K; Doud LK; Hagerman R; Pergolizzi RG; Erster SH; Thibodeau SN
    Am J Hum Genet; 1993 Dec; 53(6):1217-28. PubMed ID: 7902673
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Expansion of the fragile X CGG repeat in females with premutation or intermediate alleles.
    Nolin SL; Brown WT; Glicksman A; Houck GE; Gargano AD; Sullivan A; Biancalana V; Bröndum-Nielsen K; Hjalgrim H; Holinski-Feder E; Kooy F; Longshore J; Macpherson J; Mandel JL; Matthijs G; Rousseau F; Steinbach P; Väisänen ML; von Koskull H; Sherman SL
    Am J Hum Genet; 2003 Feb; 72(2):454-64. PubMed ID: 12529854
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Cryptic and polar variation of the fragile X repeat could result in predisposing normal alleles.
    Kunst CB; Warren ST
    Cell; 1994 Jun; 77(6):853-61. PubMed ID: 7911740
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Fragile X founder effects and new mutations in Finland.
    Zhong N; Kajanoja E; Smits B; Pietrofesa J; Curley D; Wang D; Ju W; Nolin S; Dobkin C; Ryynänen M; Brown WT
    Am J Med Genet; 1996 Jul; 64(1):226-33. PubMed ID: 8826481
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Analysis of FMR1 (CGG)(n) alleles and DXS548-FRAXAC1 haplotypes in three European circumpolar populations: traces of genetic relationship with Asia.
    Larsen LA; Vuust J; Nystad M; Evseeva I; Van Ghelue M; Tranebjaerg L
    Eur J Hum Genet; 2001 Sep; 9(9):724-7. PubMed ID: 11571563
    [TBL] [Abstract][Full Text] [Related]  

  • 15. AGG interruptions within the maternal FMR1 gene reduce the risk of offspring with fragile X syndrome.
    Yrigollen CM; Durbin-Johnson B; Gane L; Nelson DL; Hagerman R; Hagerman PJ; Tassone F
    Genet Med; 2012 Aug; 14(8):729-36. PubMed ID: 22498846
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Fragile X AGG analysis provides new risk predictions for 45-69 repeat alleles.
    Nolin SL; Sah S; Glicksman A; Sherman SL; Allen E; Berry-Kravis E; Tassone F; Yrigollen C; Cronister A; Jodah M; Ersalesi N; Dobkin C; Brown WT; Shroff R; Latham GJ; Hadd AG
    Am J Med Genet A; 2013 Apr; 161A(4):771-8. PubMed ID: 23444167
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Decrease in the CGGn trinucleotide repeat mutation of the fragile X syndrome to normal size range during paternal transmission.
    Väisänen ML; Haataja R; Leisti J
    Am J Hum Genet; 1996 Sep; 59(3):540-6. PubMed ID: 8751854
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Evidence for high-risk haplotypes and (CGG)n expansion in fragile X syndrome in the Hellenic population of Greece and Cyprus.
    Syrrou M; Patsalis PC; Georgiou I; Hadjimarcou MI; Constantinou-Deltas CD; Pagoulatos G
    Am J Med Genet; 1996 Jul; 64(1):234-8. PubMed ID: 8826482
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Detecting AGG Interruptions in Male and Female FMR1 Premutation Carriers by Single-Molecule Sequencing.
    Ardui S; Race V; Zablotskaya A; Hestand MS; Van Esch H; Devriendt K; Matthijs G; Vermeesch JR
    Hum Mutat; 2017 Mar; 38(3):324-331. PubMed ID: 27883256
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.