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151. 2p15–p16.1 microdeletion syndrome: molecular characterization and association of the OTX1 and XPO1 genes with autism spectrum disorders

153. Urinary p-cresol is elevated in small children with severe autism spectrum disorder

154. Family-based association study of ITGB3 in autism spectrum disorder and its endophenotypes

155. Principal pathogenetic components and biological endophenotypes in autism spectrum disorders

156. Mitochondrial pathways to autism

162. Clinical, Morphological, and Biochemical Correlates of Head Circumference in Autism

164. HOXA1gene variants influence head growth rates in humans

165. Case-control and family-based association studies of candidate genes in autistic disorder and its endophenotypes: TPH2 and GLO1

166. Association of a Functional Deficit of the BKCaChannel, a Synaptic Regulator of Neuronal Excitability, With Autism and Mental Retardation

173. Barrel Pattern Formation Requires Serotonin Uptake by Thalamocortical Afferents, and Not Vesicular Monoamine Release

174. No association between the 4G/5G polymorphism of the plasminogen activator inhibitor-1 gene promoter and autistic disorder

175. Methodological factors influencing measurement and processing of plasma reelin in humans

176. Differential regulation of adenosine A1 and A2A receptors in serotonin transporter and monoamine oxidase A-deficient mice

178. Adenosine deaminase alleles and autistic disorder: Case-control and family-based association studies

179. Urinary p-cresol is elevated in young French children with autism spectrum disorder: a replication study.

187. Xp22.33p22.12 Duplication in a Patient with Intellectual Disability and Dysmorphic Facial Features

191. Human μ opiate receptor

194. A human synaptic vesicle monoamine transporter cDNA predicts posttranslational modifications, reveals chromosome 10 gene localization and identifiesTaqI RFLPs

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