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Journal of Child Psychology and Psychiatry, and Allied Disciplines|June 9, 2012
Randomized controlled double-blind trial of optimal dose methylphenidate in children and adolescents with severe attention deficit hyperactivity disorder and intellectual disabilityEmily Simonoff, Eric Taylor, Gillian Baird, et al.
European Journal of Human Genetics : EJHG|February 13, 2014
Homozygous microdeletion of exon 5 in ZNF277 in a girl with specific language impairmentFabiola Ceroni, Nuala H Simpson, Clyde Francks, et al.
European Journal of Human Genetics : EJHG|August 4, 2005
Dimensional phenotypic analysis and functional categorisation of mutations reveal novel genotype-phenotype associations in Rett syndromeTony Charman, Tracey C S Neilson, Veronica Mash, et al.
Autism Research : Official Journal of the International Society for Autism Research|May 12, 2015
New Interview and Observation Measures of the Broader Autism Phenotype: Description of Strategy and Reliability Findings for the Interview MeasuresJeremy R Parr, Maretha V De Jonge, Simon Wallace, et al.
Health Technology Assessment (Winchester, England)|June 13, 2015
Systematic review of tools to measure outcomes for young children with autism spectrum disorderHelen McConachie, Jeremy R Parr, Magdalena Glod, et al.
Molecular Autism|April 11, 2017
Neurogenetic analysis of childhood disintegrative disorderAbha R Gupta, Alexander Westphal, Daniel Y J Yang, et al.
Plos Genetics|March 18, 2015
Exome sequencing in an admixed isolated population indicates NFXL1 variants confer a risk for specific language impairmentPía Villanueva, Ron Nudel, Alexander Hoischen, et al.
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