Výsledky vyhledávání - Jon Warner

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  1. 1
    A general method for the detection of large CAG repeat expansions by fluorescent PCR.

    A general method for the detection of large CAG repeat expansions by fluorescent PCR. Autor Jon Warner, L H Barron, David Goudie, K Kelly, David J. Dow, David Fitzpatrick, D. J. H. Brock

    Vydáno 1996
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    Artigo
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  2. 2
    Classification of ambiguous mutations in DNA mismatch repair genes identified in a population-based study of colorectal cancer

    Classification of ambiguous mutations in DNA mismatch repair genes identified in a population-based study of colorectal cancer Autor Rebecca A. Barnetson, Nicola Cartwright, Annelot van Vliet, Naila Haq, Kate Drew, Susan M. Farrington, Nicola Williams, Jon Warner, Harry Campbell, Mary Porteous, Malcolm G. Dunlop

    Vydáno 2007
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  3. 3
    The Edinburgh randomised trial of breast cancer screening: results after 10 years of follow-up

    The Edinburgh randomised trial of breast cancer screening: results after 10 years of follow-up Autor FE Alexander, TJ Anderson, HK Brown, APM Forrest, W Hepburn, AE Kirkpatrick, C. McDonald, BB Muir, RJ Prescott, SM Shepherd, A.F. Smith, Jon Warner

    Vydáno 1994
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  4. 4
    A second locus for hereditary hemorrhagic telangiectasia maps to chromosome 12.

    A second locus for hereditary hemorrhagic telangiectasia maps to chromosome 12. Autor David W. Johnson, Jonathan Berg, Carol J. Gallione, Kimberly A. McAllister, Jon Warner, E.A. Helmbold, Dorene S. Markel, Charles E. Jackson, Mary Porteous, Douglas A. Marchuk

    Vydáno 1995
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  5. 5
    Genetic epidemiology of motor neuron disease-associated variants in the Scottish population

    Genetic epidemiology of motor neuron disease-associated variants in the Scottish population Autor Holly A. Black, Danielle Leighton, Elaine Cleary, Elaine Rose, Laura Stephenson, Shuna Colville, David Ross, Jon Warner, Mary Porteous, George Gorrie, Robert Swingler, David B. Goldstein, Matthew Harms, Peter Connick, Suvankar Pal, Timothy J. Aitman, Siddharthan Chandran

    Vydáno 2016
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  6. 6
    De novo repeat interruptions are associated with reduced somatic instability and mild or absent clinical features in myotonic dystrophy type 1

    De novo repeat interruptions are associated with reduced somatic instability and mild or absent clinical features in myotonic dystrophy type 1 Autor Sarah A. Cumming, Mark Hamilton, Yvonne Robb, Helen Gregory, Catherine McWilliam, Anneli Cooper, Berit Adam, Josephine McGhie, Graham Hamilton, Pawel Herzyk, Michael Tschannen, Elizabeth A. Worthey, Richard Petty, Bob Ballantyne, Jon Warner, Maria Elena Farrugia, Cheryl Longman, Darren G. Monckton

    Vydáno 2018
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  7. 7
    Reduced penetrance alleles for Huntington's disease: a multi-centre direct observational study

    Reduced penetrance alleles for Huntington's disease: a multi-centre direct observational study Autor Oliver Quarrell, Alan S. Rigby, L Barron, Yanick J. Crow, A. Dalton, N R Dennis, Alan Fryer, Frances Heydon, Esther Kinning, Alison Lashwood, Monique Losekoot, L Margerison, Shannon K. McDonnell, Patrick J. Morrison, Andrew Norman, Michael Peterson, F. Lucy Raymond, Sharon Simpson, Elizabeth Thompson, Jon Warner

    Vydáno 2006
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  8. 8
    Synapse loss in the prefrontal cortex is associated with cognitive decline in amyotrophic lateral sclerosis

    Synapse loss in the prefrontal cortex is associated with cognitive decline in amyotrophic lateral sclerosis Autor Christopher M. Henstridge, Dimitrios I. Sideris, Emily Carroll, Sanziana Rotariu, Sally Salomonsson, Makis Tzioras, Chris-Anne McKenzie, Colin Smith, Christine A. F. Von Arnim, Albert C. Ludolph, Dorothée Lulé, Danielle Leighton, Jon Warner, Elaine Cleary, Judith Newton, Robert Swingler, Siddharthan Chandran, Thomas H. Gillingwater, Sharon Abrahams, Tara L. Spires‐Jones

    Vydáno 2017
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  9. 9
    Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation

    Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation Autor Patrick Tarpey, F. Lucy Raymond, Lam Son Nguyen, Jayson Rodriguez, Anna Hackett, Lucianne Vandeleur, Raffaella Smith, Cheryl Shoubridge, Sarah Edkins, Claire Stevens, Sarah O’Meara, Calli Tofts, Syd Barthorpe, Gemma Buck, Jennifer Cole, Kelly Halliday, Katy Hills, David Jones, Tatiana Mironenko, Janet Perry, Jennifer Varian, Sofie West, Sara Widaa, John Teague, Ed Dicks, Adam P. Butler, Andrew Menzies, David Richardson, Andy Jenkinson, Rebecca Shepherd, Keiran Raine, Jenny Moon, Yin Luo, Josep Parnau, Shambhu S. Bhat, Alison Gardner, Mark Corbett, Doug A. Brooks, Paul Q. Thomas, Emma J. Parkinson-Lawrence, Mary Porteous, Jon Warner, T. L. Sanderson, Pauline Pearson, Richard J. Simensen, Cindy Skinner, George Hoganson, Duane Superneau, Richard Wooster, Martin Bobrow, Gillian Turner, Roger E. Stevenson, Charles E. Schwartz, P. Andrew Futreal, Anand Srivastava, Michael R. Stratton, Jozef Gécz

    Vydáno 2007
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