Showing 1 - 9 results of 9 for search 'Copp, A', query time: 0.04s
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FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder. by Lai, C, Gerrelli, D, Monaco, A, Fisher, S, Copp, A
Published 2003Journal article -
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Is LMNB1 a susceptibility gene for neural tube defects in humans? by Robinson, A, Partridge, D, Malhas, A, De Castro, S, Gustavsson, P, Thompson, D, Vaux, D, Copp, A, Stanier, P, Bassuk, A, Greene, N
Published 2013Journal article -
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The Meckel-Gruber Syndrome proteins MKS1 and meckelin interact and are required for primary cilium formation. by Dawe, H, Smith, U, Cullinane, A, Gerrelli, D, Cox, P, Badano, J, Blair-Reid, S, Sriram, N, Katsanis, N, Attie-Bitach, T, Afford, S, Copp, A, Kelly, D, Gull, K, Johnson, C
Published 2007Journal article -
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The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration. by Paracchini, S, Thomas, A, Castro, S, Lai, C, Paramasivam, M, Wang, Y, Keating, B, Taylor, J, Hacking, D, Scerri, T, Francks, C, Richardson, A, Wade-Martins, R, Stein, J, Knight, J, Copp, A, Loturco, J, Monaco, A
Published 2006Journal article -
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The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration by Paracchini, S, Thomas, A, Castro, S, Lai, C, Paramasivam, M, Wang, Y, Keating, B, Taylor, J, Hacking, D, Scerri, T, Francks, C, Richardson, A, Wade-Martins, R, Stein, J, Knight, J, Copp, A, LoTurco, J, Monaco, A
Published 2006Journal article