Strong association of de novo copy number mutations with autism.

Sebat J, Lakshmi B, Malhotra D, Troge J, Lese-Martin C, Walsh T, Yamrom B, Yoon S, Krasnitz A, Kendall J, Leotta A, Pai D, Zhang R, Lee YH, Hicks J, Spence SJ, Lee AT, Puura K, Lehtimäki T, Ledbetter D, Gregersen PK, Bregman J, Sutcliffe JS, Jobanputra V, Chung W, Warburton D, King MC, Skuse D, Geschwind DH, Gilliam TC, Ye K, Wigler M
Science. 2007 316 (5823): 445-9

PMID: 17363630 · PMCID: PMC2993504 · DOI:10.1126/science.1138659

MeSH Terms (22)

Asperger Syndrome Autistic Disorder Case-Control Studies Child Cytogenetic Analysis Female Gene Deletion Gene Dosage Gene Duplication Genetic Predisposition to Disease Genome, Human Germ-Line Mutation Humans In Situ Hybridization, Fluorescence Male Markov Chains Microsatellite Repeats Mutation Nucleic Acid Hybridization Oligonucleotide Array Sequence Analysis Parents Siblings

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