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Common genetic variants, acting additively, are a major source of risk for autism
Download from link.springer.comA balanced t(10;15) translocation in a male patient with developmental language disorder
Download from www.ncbi.nlm.nih.govSearching for Potocki-Lupski syndrome Phenotype: A Patient with Language Impairment and no Autism
Download from www.ncbi.nlm.nih.govDeletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia
Download from www.ncbi.nlm.nih.govWhole exome sequencing identifies recessive WDR62 mutations in severe brain malformations
Download from www.nature.coml-Histidine Decarboxylase and Tourette's Syndrome
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