檢索結果 - 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 由 David Hunt, Richard J. Leventer, Cas Simons, Ryan J. Taft, Kathryn J. Swoboda, M. L. Gawne‐Cain, Alex Magee, Peter D. Turnpenny, Diana Baralle

    出版 2014
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    Progressive cerebral atrophy in multiple sclerosis A serial MRI study

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

    出版 1996
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    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. 由 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

    出版 1996
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    Anatomical subgroup analysis of the MERIDIAN cohort: ventriculomegaly

    Anatomical subgroup analysis of the MERIDIAN cohort: ventriculomegaly 由 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

    出版 2017
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