{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,24]],"date-time":"2026-07-24T14:19:22Z","timestamp":1784902762749,"version":"3.55.0"},"reference-count":10,"publisher":"Elsevier BV","issue":"3","license":[{"start":{"date-parts":[[2016,6,1]],"date-time":"2016-06-01T00:00:00Z","timestamp":1464739200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2016,6,1]],"date-time":"2016-06-01T00:00:00Z","timestamp":1464739200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"}],"content-domain":{"domain":["clinicalkey.com","clinicalkey.com.au","clinicalkey.es","clinicalkey.fr","clinicalkey.jp","jaapos.org","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Journal of American Association for Pediatric Ophthalmology and Strabismus"],"published-print":{"date-parts":[[2016,6]]},"DOI":"10.1016\/j.jaapos.2016.02.003","type":"journal-article","created":{"date-parts":[[2016,4,29]],"date-time":"2016-04-29T07:29:35Z","timestamp":1461914975000},"page":"278-280","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":9,"title":["Ocular findings associated with chromosome 22q11.2 duplication"],"prefix":"10.1016","volume":"20","author":[{"given":"Brian J.","family":"Forbes","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Donna M.","family":"McDonald-McGinn","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Georgia","family":"Wootton","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Lindsay","family":"Dawson","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Elaine","family":"Zackai","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Gil","family":"Binenbaum","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1016\/j.jaapos.2016.02.003_bib1","doi-asserted-by":"crossref","first-page":"489","DOI":"10.1093\/hmg\/9.4.489","article-title":"Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis","volume":"9","author":"Shaikh","year":"2000","journal-title":"Hum Mol Genet"},{"key":"10.1016\/j.jaapos.2016.02.003_bib2","first-page":"11","article-title":"The Philadelphia story: the 22q11.2 deletion: report on 250 patients","volume":"10","author":"McDonald-McGinn","year":"1999","journal-title":"Genet Couns"},{"key":"10.1016\/j.jaapos.2016.02.003_bib3","doi-asserted-by":"crossref","first-page":"801","DOI":"10.1002\/pd.4613","article-title":"Prevalence of recurrent pathogenic microdeletions and microduplications in over 9,500 pregnancies","volume":"35","author":"Grati","year":"2015","journal-title":"Prenat Diagn"},{"key":"10.1016\/j.jaapos.2016.02.003_bib4","doi-asserted-by":"crossref","first-page":"1027","DOI":"10.1086\/378818","article-title":"Microduplication 22q11.2, an emerging syndrome: clinical, cytogenetic, and molecular analysis of thirteen patients","volume":"73","author":"Ensenauer","year":"2003","journal-title":"Am J Hum Genet"},{"key":"10.1016\/j.jaapos.2016.02.003_bib5","doi-asserted-by":"crossref","first-page":"e67","DOI":"10.1590\/S0066-782X2009001000025","article-title":"22q11. 2 duplication and congenital heart defects","volume":"93","author":"Rosa","year":"2009","journal-title":"Arq Bras Cardiol"},{"key":"10.1016\/j.jaapos.2016.02.003_bib6","doi-asserted-by":"crossref","first-page":"35","DOI":"10.1002\/pd.4478","article-title":"Prenatal diagnosis of 24 cases of microduplication 22q11.2: an investigation of phenotype-genotype correlations","volume":"35","author":"Dupont","year":"2015","journal-title":"Prenat Diagn"},{"key":"10.1016\/j.jaapos.2016.02.003_bib7","first-page":"179","article-title":"Ocular findings in the chromosome 22q11.2 deletion syndrome","volume":"11","author":"Forbes","year":"2007","journal-title":"J\u00a0AAPOS"},{"key":"10.1016\/j.jaapos.2016.02.003_bib8","doi-asserted-by":"crossref","first-page":"904","DOI":"10.1002\/ajmg.a.32156","article-title":"Sclerocornea associated with the chromosome 22q11.2 deletion syndrome","volume":"146A","author":"Binenbaum","year":"2008","journal-title":"Am J Med Genet A"},{"key":"10.1016\/j.jaapos.2016.02.003_bib9","doi-asserted-by":"crossref","first-page":"392","DOI":"10.1016\/j.ophtha.2013.06.040","article-title":"Ocular manifestations of 22q11. 2 microduplication","volume":"121","author":"Cordovez","year":"2014","journal-title":"Ophthalmology"},{"key":"10.1016\/j.jaapos.2016.02.003_bib10","doi-asserted-by":"crossref","first-page":"501","DOI":"10.1016\/j.ejmg.2008.07.005","article-title":"Clinical variability of the 22q11.2 duplication syndrome","volume":"51","author":"Wentzel","year":"2008","journal-title":"Eur J Med Genet"}],"container-title":["Journal of American Association for Pediatric Ophthalmology and Strabismus"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1091853116300477?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1091853116300477?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,10,21]],"date-time":"2025-10-21T20:21:55Z","timestamp":1761078115000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S1091853116300477"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2016,6]]},"references-count":10,"journal-issue":{"issue":"3","published-print":{"date-parts":[[2016,6]]}},"alternative-id":["S1091853116300477"],"URL":"https:\/\/doi.org\/10.1016\/j.jaapos.2016.02.003","relation":{},"ISSN":["1091-8531"],"issn-type":[{"value":"1091-8531","type":"print"}],"subject":[],"published":{"date-parts":[[2016,6]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Ocular findings associated with chromosome 22q11.2 duplication","name":"articletitle","label":"Article Title"},{"value":"Journal of American Association for Pediatric Ophthalmology and Strabismus","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.jaapos.2016.02.003","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"Copyright \u00a9 2016 by the American Association for Pediatric Ophthalmology and Strabismus.","name":"copyright","label":"Copyright"}]}}