Showing 1 - 6 results of 6 for search 'Patrick F Bolton', query time: 0.04s Refine Results
  1. 1
    A comparison of two studies and the prevalence and sex ratio of Neurodevelopmental conditions in Tuberous Sclerosis Complex

    A comparison of two studies and the prevalence and sex ratio of Neurodevelopmental conditions in Tuberous Sclerosis Complex by Abigail K. Runicles, Charlotte Tye, Patrick F. Bolton

    Published 2021-08-01
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  2. 2
    Traits contributing to the autistic spectrum.

    Traits contributing to the autistic spectrum. by Colin D Steer, Jean Golding, Patrick F Bolton

    Published 2010-09-01
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  3. 3
    Actigraph-Measured Movement Correlates of Attention-Deficit/Hyperactivity Disorder (ADHD) Symptoms in Young People with Tuberous Sclerosis Complex (TSC) with and without Intellectual Disability and Autism Spectrum Disorder (ASD)

    Actigraph-Measured Movement Correlates of Attention-Deficit/Hyperactivity Disorder (ADHD) Symptoms in Young People with Tuberous Sclerosis Complex (TSC) with and without Intellectu... by Tom Earnest, Elizabeth Shephard, Charlotte Tye, Fiona McEwen, Emma Woodhouse, Holan Liang, Fintan Sheerin, Patrick F. Bolton

    Published 2020-07-01
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  4. 4
    Exome sequencing in an admixed isolated population indicates NFXL1 variants confer a risk for specific language impairment.

    Exome sequencing in an admixed isolated population indicates NFXL1 variants confer a risk for specific language impairment. by Pía Villanueva, Ron Nudel, Alexander Hoischen, María Angélica Fernández, Nuala H Simpson, Christian Gilissen, Rose H Reader, Lillian Jara, María Magdalena Echeverry, Clyde Francks, Gillian Baird, Gina Conti-Ramsden, Anne O'Hare, Patrick F Bolton, Elizabeth R Hennessy, SLI Consortium, Hernán Palomino, Luis Carvajal-Carmona, Joris A Veltman, Jean-Baptiste Cazier, Zulema De Barbieri, Simon E Fisher, Dianne F Newbury

    Published 2015-03-01
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  5. 5
    Correction: Exome Sequencing in an Admixed Isolated Population Indicates NFXL1 Variants Confer a Risk for Specific Language Impairment.

    Correction: Exome Sequencing in an Admixed Isolated Population Indicates NFXL1 Variants Confer a Risk for Specific Language Impairment. by Pía Villanueva, Ron Nudel, Alexander Hoischen, María Angélica Fernández, Nuala H Simpson, Christian Gilissen, Rose H Reader, Lillian Jara, María Magdalena Echeverry, Clyde Francks, Gillian Baird, Gina Conti-Ramsden, Anne O'Hare, Patrick F Bolton, Elizabeth R Hennessy, SLI Consortium, Hernán Palomino, Luis Carvajal-Carmona, Joris A Veltman, Jean-Baptiste Cazier, Zulema De Barbieri, Simon E Fisher, Dianne F Newbury

    Published 2015-06-01
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  6. 6
    Tuberous Sclerosis Complex (TSC): Expert Recommendations for Provision of Coordinated Care

    Tuberous Sclerosis Complex (TSC): Expert Recommendations for Provision of Coordinated Care by Nicholas M. P. Annear, Nicholas M. P. Annear, Richard E. Appleton, Zahabiyah Bassi, Rupesh Bhatt, Patrick F. Bolton, Pamela Crawford, Alex Crowe, Maureen Tossi, Maureen Tossi, Frances Elmslie, Frances Elmslie, Eric Finlay, Daniel P. Gale, Alex Henderson, Elizabeth A. Jones, Elizabeth A. Jones, Simon R. Johnson, Simon R. Johnson, Shelagh Joss, Larissa Kerecuk, Graham Lipkin, Patrick J. Morrison, Finbar J. O'Callaghan, Jill Cadwgan, Jill Cadwgan, Jill Cadwgan, Albert C. M. Ong, Albert C. M. Ong, Julian R. Sampson, Charles Shepherd, J. Chris Kingswood, J. Chris Kingswood, J. Chris Kingswood

    Published 2019-11-01
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