Search Results - M. L. Gawne‐Cain

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  1. 1
    Whole exome sequencing in family trios reveals<i>de novo</i>mutations in<i>PURA</i>as a cause of severe neurodevelopmental delay and learning disability

    Whole exome sequencing in family trios reveals<i>de novo</i>mutations in<i>PURA</i>as a cause of severe neurodevelopmental delay and learning disability by David Hunt, Richard J. Leventer, Cas Simons, Ryan J. Taft, Kathryn J. Swoboda, M. L. Gawne‐Cain, Alex Magee, Peter D. Turnpenny, Diana Baralle

    Published 2014
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  2. 2
    Progressive cerebral atrophy in multiple sclerosis A serial MRI study

    Progressive cerebral atrophy in multiple sclerosis A serial MRI study by N. A. Losseff, L. Wang, Hsi‐Mei Lai, Dong Soo Yoo, M. L. Gawne‐Cain, W. I. McDonald, D. H. Miller, Alan J. Thompson

    Published 1996
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  3. 3
    A preliminary study into the sensitivity of disease activity detection by serial weekly magnetic resonance imaging in multiple sclerosis.

    A preliminary study into the sensitivity of disease activity detection by serial weekly magnetic resonance imaging in multiple sclerosis. by Mitchell K.P. Lai, Timothy J. Hodgson, M. L. Gawne‐Cain, Stephen A. Webb, David MacManus, W. I. McDonald, Alan J. Thompson, David H. Miller

    Published 1996
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  4. 4
    Anatomical subgroup analysis of the MERIDIAN cohort: ventriculomegaly

    Anatomical subgroup analysis of the MERIDIAN cohort: ventriculomegaly by Paul D. Griffiths, K. Brackley, Mike Bradburn, Daniel Connolly, M. L. Gawne‐Cain, Dylan Griffiths, Mark D. Kilby, Laura Mandefield, Cara Mooney, Stephen C. Robson, Brigitte Vollmer, Gerald Mason

    Published 2017
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