{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,7]],"date-time":"2026-08-07T16:31:28Z","timestamp":1786120288322,"version":"build-2736575974"},"reference-count":12,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"8","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2011,10]]},"DOI":"10.1097\/dbp.0b013e31823299d6","type":"journal-article","created":{"date-parts":[[2011,10,4]],"date-time":"2011-10-04T15:58:25Z","timestamp":1317743905000},"page":"600-604","source":"Crossref","is-referenced-by-count":6,"title":["Craniofacial Dysmorphism and Developmental Disorders Among Children with Chromosomal Microdeletions and Duplications of Unknown Significance"],"prefix":"10.1097","volume":"32","author":[{"given":"William T.","family":"Gannon","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jose E.","family":"Martinez","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Stephanie J.","family":"Anderson","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Hanes M.","family":"Swingle","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"276","reference":[{"key":"R1-7-20210129","doi-asserted-by":"crossref","first-page":"1183","DOI":"10.1542\/peds.2007-2361","article-title":"Identification and evaluation of children with autism spectrum disorders.","volume":"120","author":"Johnson","year":"2007","journal-title":"Pediatrics"},{"key":"R2-7-20210129","doi-asserted-by":"crossref","first-page":"468","DOI":"10.1212\/WNL.55.4.468","article-title":"Practice parameter: screening and diagnosis of autism: report of the Quality Standards Subcommittee of the American Academy of Neurology and the Child Neurology Society.","volume":"55","author":"Filipek","year":"2000","journal-title":"Neurology"},{"key":"R3-7-20210129","doi-asserted-by":"crossref","first-page":"749","DOI":"10.1016\/j.ajhg.2010.04.006","article-title":"Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.","volume":"86","author":"Miller","year":"2010","journal-title":"Am J Hum Genet"},{"key":"R4-7-20210129","doi-asserted-by":"crossref","first-page":"e727","DOI":"10.1542\/peds.2009-1684","article-title":"Clinical genetic testing for patients with autism spectrum disorders.","volume":"125","author":"Shen","year":"2010","journal-title":"Pediatrics"},{"key":"R6-7-20210129","doi-asserted-by":"crossref","first-page":"36","DOI":"10.1159\/000184690","article-title":"The role of rare structural variants in the genetics of autism spectrum disorders.","volume":"123","author":"Kusenda","year":"2008","journal-title":"Cytogenet Genome Res"},{"key":"R7-7-20210129","doi-asserted-by":"crossref","first-page":"445","DOI":"10.1126\/science.1138659","article-title":"Strong association of de novo copy number mutations with autism.","volume":"316","author":"Sebat","year":"2007","journal-title":"Science"},{"key":"R8-7-20210129","doi-asserted-by":"crossref","first-page":"245","DOI":"10.1002\/(SICI)1096-8628(20000410)91:4<245::AID-AJMG1>3.0.CO;2-2","article-title":"Value of a clinical morphology examination in autism.","volume":"91","author":"Miles","year":"2000","journal-title":"Am J Med Genet"},{"key":"R9-7-20210129","doi-asserted-by":"crossref","first-page":"171","DOI":"10.1002\/ajmg.a.30590","article-title":"Essential versus complex autism: definition of fundamental prognostic subtypes.","volume":"135","author":"Miles","year":"2005","journal-title":"Am J Med Genet A"},{"key":"R10-7-20210129","doi-asserted-by":"crossref","first-page":"1101","DOI":"10.1002\/ajmg.a.32244","article-title":"Development and validation of a measure of dysmorphology: useful for autism subgroup classification.","volume":"146A","author":"Miles","year":"2008","journal-title":"Am J Med Genet A"},{"key":"R11-7-20210129","doi-asserted-by":"crossref","first-page":"204","DOI":"10.2353\/jmoldx.2010.090115","article-title":"Genome-wide oligonucleotide array comparative genomic hybridization for etiological diagnosis of mental retardation: a multicenter experience of 1499 clinical cases.","volume":"12","author":"Xiang","year":"2010","journal-title":"J Mol Diagn"},{"key":"R12-7-20210129","article-title":"Diagnostic and Statistical Manual of Mental Disorders: DSM-IV-TR.","year":"2000"},{"key":"R13-7-20210129","doi-asserted-by":"crossref","first-page":"205","DOI":"10.1023\/A:1005592401947","article-title":"The Autism Diagnostic Observation Schedule-Generic: a standard measure of social and communication deficits associated with the spectrum of autism.","volume":"30","author":"Lord","year":"2000","journal-title":"J Autism Dev Disord"}],"container-title":["Journal of Developmental &amp; Behavioral Pediatrics"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.ovid.com\/00004703-201110000-00007","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2026,8,6]],"date-time":"2026-08-06T20:27:15Z","timestamp":1786048035000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.ovid.com\/00004703-201110000-00007"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2011,10]]},"references-count":12,"journal-issue":{"issue":"8","published-print":{"date-parts":[[2011]]}},"URL":"https:\/\/doi.org\/10.1097\/dbp.0b013e31823299d6","relation":{},"ISSN":["0196-206X"],"issn-type":[{"value":"0196-206X","type":"print"}],"subject":[],"published":{"date-parts":[[2011,10]]}}}