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Journal of Autism and Developmental Disorders|February 12, 2013
How to use the ADI-R for classifying autism spectrum disorders? Psychometric properties of criteria from the literature in 1,204 Dutch childrenAnnelies de Bildt, Iris J Oosterling, Natasja D J van Lang, et al.European Journal of Cancer (Oxford, England : 1990)|January 29, 2016
Diffuse large B-cell lymphoma with MYC gene rearrangements: Current perspective on treatment of diffuse large B-cell lymphoma with MYC gene rearrangements; case series and review of the literatureA V de Jonge, T J A Roosma, I Houtenbos, 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.Neurogenetics|August 13, 2011
Social Responsiveness Scale-aided analysis of the clinical impact of copy number variations in autismEmma van Daalen, Chantal Kemner, Nienke E Verbeek, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|June 10, 2011
No association between a common single nucleotide polymorphism, rs4141463, in the MACROD2 gene and autism spectrum disorderSarah Curran, Patrick Bolton, Kinga Rozsnyai, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 24, 2009
A co-segregating microduplication of chromosome 15q11.2 pinpoints two risk genes for autism spectrum disorderBert van der Zwaag, Wouter G Staal, Ron Hochstenbach, et al.Journal of Autism and Developmental Disorders|February 16, 2015
Autism Diagnostic Interview-Revised (ADI-R) Algorithms for Toddlers and Young Preschoolers: Application in a Non-US Sample of 1,104 ChildrenAnnelies de Bildt, Sjoerd Sytema, Eric Zander, et al.Neurogenetics|January 22, 2013
Clinical and genetic aspects of PCDH19-related epilepsy syndromes and the possible role of PCDH19 mutations in males with autism spectrum disordersJ J T van Harssel, S Weckhuysen, M J A van Kempen, et al.Biological Psychiatry|March 30, 2010
Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexiaAlistair T Pagnamenta, Elena Bacchelli, Maretha V de Jonge, et al.Plos One|June 4, 2009
Gene-network analysis identifies susceptibility genes related to glycobiology in autismBert van der Zwaag, Lude Franke, Martin Poot, et al.Pageof 5