Strong Association of De Novo Copy Number Mutations with Autism - Sebat, Jonathan; Lakshmi, B; Malhotra, Dheeraj; Troge, Jennifer; Lese-Martin, Christa; Walsh, Tom; Yamrom, Boris; Yoon, Seungtai; Krasnitz, Alex; Kendall, Jude; Leotta, Anthony; Pai, Deepa; et al. (Science (American Association for the Advancement of Science), 2007)
Keywords: Asperger Syndrome - genetics; Autism; Autism Spectrum Disorders; Autistic disorder; Autistic Disorder - genetics; Biological and medical sciences; Case-Control Studies; Child; Child clinical studies; Comparative genomic hybridization; Cytogenetic Analysis; cytogenetics; Deoxyribonucleic acid; Developmental disorders; DNA; Female; Fluorescence in situ hybridization; Gene Deletion; Gene Dosage; Gene Duplication; Genes; Genetic markers; Genetic mutation; Genetic Predisposition to Disease; Genome, Human; Genomes; Genomics; genotyping; germ cells; Germ-Line Mutation; Human genetics; Humans; Hybridization; Hypothesis testing; In Situ Hybridization, Fluorescence; Infantile autism; Male; Markov Chains; Medical genetics; Medical sciences; Microsatellite Repeats; Mutation; Nucleic Acid Hybridization; Oligonucleotide Array Sequence Analysis; Parents; paternity; Patients; Pervasive child development disorders; Psychology. Psychoanalysis. Psychiatry; Psychopathology. Psychiatry; Risk factors; Siblings; Human; Autism; Family study; Copy number; Genetics; Developmental disorder; Mutation; Genetic determinism; Child; De novo