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Journal of Autism and Developmental Disorders|March 7, 2007
Sleep in children with Asperger syndromeE Juulia Paavonen, Kimmo Vehkalahti, Raija Vanhala, et al.
Nordic Journal of Psychiatry|December 24, 2013
The incidence of diagnosed autism spectrum disorders in FinlandSusanna Hinkka-Yli-Salomäki, P Nina Banerjee, Mika Gissler, et al.
European Journal of Human Genetics : EJHG|October 8, 2004
Family-based association study of DYX1C1 variants in autismTero Ylisaukko-Oja, Myriam Peyrard-Janvid, Cecilia M Lindgren, et al.
Autism Research : Official Journal of the International Society for Autism Research|March 9, 2011
Fine mapping of Xq11.1-q21.33 and mutation screening of RPS6KA6, ZNF711, ACSL4, DLG3, and IL1RAPL2 for autism spectrum disorders (ASD)Katri Kantojärvi, Ilona Kotala, Karola Rehnström, et al.
American Journal of Human Genetics|August 23, 2002
A genomewide screen for autism-spectrum disorders: evidence for a major susceptibility locus on chromosome 3q25-27Mari Auranen, Raija Vanhala, Teppo Varilo, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|November 28, 2008
Allelic variants in HTR3C show association with autismKarola Rehnström, Tero Ylisaukko-oja, Ilona Nummela, et al.
Developmental Medicine and Child Neurology|September 10, 2014
The association between congenital anomalies and autism spectrum disorders in a Finnish national birth cohortLaura Timonen-Soivio, Raija Vanhala, Heli Malm, et al.
American Journal of Medical Genetics. Part A|December 4, 2004
MECP2 mutation analysis in patients with mental retardationTero Ylisaukko-Oja, Karola Rehnström, Raija Vanhala, et al.
Annals of Neurology|November 17, 2005
Search for autism loci by combined analysis of Autism Genetic Resource Exchange and Finnish familiesTero Ylisaukko-oja, Maricela Alarcón, Rita M Cantor, et al.
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