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 *

143 related articles for article (PubMed ID: 1677119)

  • 81. Fragile sites, chromosomal lesions, tandem repeats, and disease.
    Mirceta M; Shum N; Schmidt MHM; Pearson CE
    Front Genet; 2022; 13():985975. PubMed ID: 36468036
    [TBL] [Abstract][Full Text] [Related]  

  • 82. Advancing genomic technologies and clinical awareness accelerates discovery of disease-associated tandem repeat sequences.
    Gall-Duncan T; Sato N; Yuen RKC; Pearson CE
    Genome Res; 2022 Jan; 32(1):1-27. PubMed ID: 34965938
    [TBL] [Abstract][Full Text] [Related]  

  • 83. Zebrafish Chromosome 14 Gene Differential Expression in the
    Barthelson K; Baer L; Dong Y; Hand M; Pujic Z; Newman M; Goodhill GJ; Richards RI; Pederson SM; Lardelli M
    Front Genet; 2021; 12():625466. PubMed ID: 34135935
    [TBL] [Abstract][Full Text] [Related]  

  • 84. The Contribution of Somatic Expansion of the CAG Repeat to Symptomatic Development in Huntington's Disease: A Historical Perspective.
    Monckton DG
    J Huntingtons Dis; 2021; 10(1):7-33. PubMed ID: 33579863
    [TBL] [Abstract][Full Text] [Related]  

  • 85. Ratiometric Fluorescence Detection of DNA Based on the Inner Filter Effect of Ru(bpy)
    Zhang Y; Hou D; Zhao B; Li C; Wang X; Xu L; Long T
    ACS Omega; 2021 Jan; 6(1):857-862. PubMed ID: 33458536
    [TBL] [Abstract][Full Text] [Related]  

  • 86. Epilepsy in families: Age at onset is a familial trait, independent of syndrome.
    Ellis CA; Churilov L; Epstein MP; Xie SX; Bellows ST; Ottman R; Berkovic SF;
    Ann Neurol; 2019 Jul; 86(1):91-98. PubMed ID: 31050039
    [TBL] [Abstract][Full Text] [Related]  

  • 87. The overdue promise of short tandem repeat variation for heritability.
    Press MO; Carlson KD; Queitsch C
    Trends Genet; 2014 Nov; 30(11):504-12. PubMed ID: 25182195
    [TBL] [Abstract][Full Text] [Related]  

  • 88. The unstable repeats--three evolving faces of neurological disease.
    Nelson DL; Orr HT; Warren ST
    Neuron; 2013 Mar; 77(5):825-43. PubMed ID: 23473314
    [TBL] [Abstract][Full Text] [Related]  

  • 89. Anticipation in hereditary disease: the history of a biomedical concept.
    Friedman JE
    Hum Genet; 2011 Dec; 130(6):705-14. PubMed ID: 21667285
    [TBL] [Abstract][Full Text] [Related]  

  • 90. Exceptional matters.
    Peters K
    Lancet; 2004 Dec 11-17; 364(9451):2142-51. PubMed ID: 15589313
    [No Abstract]   [Full Text] [Related]  

  • 91. The fragile X syndrome: no evidence for any recent mutations.
    Smits AP; Dreesen JC; Post JG; Smeets DF; de Die-Smulders C; Spaans-van der Bijl T; Govaerts LC; Warren ST; Oostra BA; van Oost BA
    J Med Genet; 1993 Feb; 30(2):94-6. PubMed ID: 8445628
    [TBL] [Abstract][Full Text] [Related]  

  • 92. Allelic instability in mitosis: a unified model for dominant disorders.
    Zheng CJ; Byers B; Moolgavkar SH
    Proc Natl Acad Sci U S A; 1993 Nov; 90(21):10178-82. PubMed ID: 8234274
    [TBL] [Abstract][Full Text] [Related]  

  • 93. Over-representation of the disease associated (CAG) and (CGG) repeats in the human genome.
    Han J; Hsu C; Zhu Z; Longshore JW; Finley WH
    Nucleic Acids Res; 1994 May; 22(9):1735-40. PubMed ID: 8202379
    [TBL] [Abstract][Full Text] [Related]  

  • 94. Dynamic mutations on the move.
    Sutherland GR; Richards RI
    J Med Genet; 1993 Dec; 30(12):978-81. PubMed ID: 8133507
    [No Abstract]   [Full Text] [Related]  

  • 95. Instability of CAG repeats in Huntington's disease: relation to parental transmission and age of onset.
    Trottier Y; Biancalana V; Mandel JL
    J Med Genet; 1994 May; 31(5):377-82. PubMed ID: 8064815
    [TBL] [Abstract][Full Text] [Related]  

  • 96. Heritable trinucleotide repeats and neurological disorders.
    Shastry BS
    Experientia; 1994 Nov; 50(11-12):1099-105. PubMed ID: 7988670
    [TBL] [Abstract][Full Text] [Related]  

  • 97. Simple tandem DNA repeats and human genetic disease.
    Sutherland GR; Richards RI
    Proc Natl Acad Sci U S A; 1995 Apr; 92(9):3636-41. PubMed ID: 7731957
    [TBL] [Abstract][Full Text] [Related]  

  • 98. Genetic analysis of kifafa, a complex familial seizure disorder.
    Neuman RJ; Kwon JM; Jilek-Aall L; Rwiza HT; Rice JP; Goodfellow PJ
    Am J Hum Genet; 1995 Oct; 57(4):902-10. PubMed ID: 7573052
    [TBL] [Abstract][Full Text] [Related]  

  • 99. Cloning of the gene for the fragile X syndrome: implications for the clinical geneticist.
    Connor JM
    J Med Genet; 1991 Dec; 28(12):811-3. PubMed ID: 1757954
    [No Abstract]   [Full Text] [Related]  

  • 100. Anticipation legitimized: unstable DNA to the rescue.
    Sutherland GR; Richards RI
    Am J Hum Genet; 1992 Jul; 51(1):7-9. PubMed ID: 1609807
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.