Search Results - Barnett, Christopher, MBBS

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  1. 1
    Characterisation of mutations of the phosphoinositide-3-kinase regulatory subunit, PIK3R2 , in perisylvian polymicrogyria: a next-generation sequencing study

    Characterisation of mutations of the phosphoinositide-3-kinase regulatory subunit, PIK3R2 , in perisylvian polymicrogyria: a next-generation sequencing study by Mirzaa, Ghayda M, Dr, Conti, Valerio, PhD, Timms, Andrew E, PhD, Smyser, Christopher D, MD, Ahmed, Sarah, MD, Carter, Melissa, MD, Barnett, Sarah, MS, Hufnagel, Robert B, MD, Goldstein, Amy, MD, Narumi-Kishimoto, Yoko, MD, Olds, Carissa, MSc, Collins, Sarah, MS, Johnston, Kathreen, MD, Deleuze, Jean-François, PhD, Nitschké, Patrick, PhD, Friend, Kathryn, PhD, Harris, Catharine, MD, Goetsch, Allison, MS, Martin, Beth, BS, Boyle, Evan August, BS, Parrini, Elena, MD, Mei, Davide, MSLT, Tattini, Lorenzo, PhD, Slavotinek, Anne, Prof, Blair, Ed, MRCP, Barnett, Christopher, MBBS, Shendure, Jay, Prof, Chelly, Jamel, Prof, Dobyns, William B, Prof, Guerrini, Renzo, Prof

    Published in Lancet neurology
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  2. 2
    8q13.1-q13.2 Deletion Associated With Inferior Cerebellar Vermian Hypoplasia and Digital Anomalies: A New Syndrome?

    8q13.1-q13.2 Deletion Associated With Inferior Cerebellar Vermian Hypoplasia and Digital Anomalies: A New Syndrome? by Mordaunt, Dylan, MB, ChB, Oftedal, Bergithe E., PhD, McLauchlan, Alisha, BSc(hons), Coates, Danika, MBBS, Waters, Wendy, BMedLabSc, Scott, Hamish, PhD, Barnett, Christopher, MBBS

    Published in Pediatric neurology
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  3. 3
    Novel Clinical Features in Pontine Tegmental Cap Dysplasia

    Novel Clinical Features in Pontine Tegmental Cap Dysplasia by Rudaks, Laura I, Patel, Sandeep, MBBS, Barnett, Christopher P., MBBS

    Published in Pediatric neurology
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  4. 4
    Novel TSEN54 Mutation Causing Pontocerebellar Hypoplasia Type 4

    Novel TSEN54 Mutation Causing Pontocerebellar Hypoplasia Type 4 by Rudaks, Laura I, Moore, Lynette, MBBS, Shand, Karen L., BMBS, Wilkinson, Christopher, BMed, Barnett, Christopher P., MBBS

    Published in Pediatric neurology
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