{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,29]],"date-time":"2025-10-29T10:20:29Z","timestamp":1761733229440,"version":"build-2065373602"},"reference-count":10,"publisher":"Elsevier BV","issue":"6","license":[{"start":{"date-parts":[[2008,11,1]],"date-time":"2008-11-01T00:00:00Z","timestamp":1225497600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2008,11,1]],"date-time":"2008-11-01T00:00:00Z","timestamp":1225497600000},"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","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["European Journal of Medical Genetics"],"published-print":{"date-parts":[[2008,11]]},"DOI":"10.1016\/j.ejmg.2008.06.004","type":"journal-article","created":{"date-parts":[[2008,7,14]],"date-time":"2008-07-14T18:15:44Z","timestamp":1216059344000},"page":"679-684","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":20,"title":["Complex constitutional subtelomeric 1p36.3 deletion\/duplication in a mentally retarded child with neonatal neuroblastoma"],"prefix":"10.1016","volume":"51","author":[{"given":"Bertrand","family":"Isidor","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Martine","family":"Le Cunff","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Michelle","family":"Boceno","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Pierre","family":"Boisseau","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Caroline","family":"Thomas","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jean-Marie","family":"Rival","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Albert","family":"David","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"C\u00e9dric","family":"Le Caignec","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.ejmg.2008.06.004_bib1","doi-asserted-by":"crossref","first-page":"657","DOI":"10.1136\/jmg.36.9.657","article-title":"Monosomy 1p36","volume":"36","author":"Slavotinek","year":"1999","journal-title":"J. Med. Genet."},{"key":"10.1016\/j.ejmg.2008.06.004_bib2","first-page":"176","article-title":"Constitutional 1p36 deletion in a child with neuroblastoma","volume":"52","author":"Biegel","year":"1993","journal-title":"Am. J. Hum. Genet."},{"key":"10.1016\/j.ejmg.2008.06.004_bib3","doi-asserted-by":"crossref","first-page":"1957","DOI":"10.1016\/S0959-8049(97)00311-0","article-title":"Molecular analysis of the region of distal 1p commonly deleted in neuroblastoma","volume":"33","author":"White","year":"1997","journal-title":"Eur. J. Cancer"},{"key":"10.1016\/j.ejmg.2008.06.004_bib4","doi-asserted-by":"crossref","first-page":"2684","DOI":"10.1038\/sj.onc.1208306","article-title":"Definition and characterization of a region of 1p36.3 consistently deleted in neuroblastoma","volume":"24","author":"White","year":"2005","journal-title":"Oncogene"},{"key":"10.1016\/j.ejmg.2008.06.004_bib5","series-title":"Principles and Practice of Pediatric Oncology","first-page":"933","article-title":"Neuroblastoma","author":"Brodeur","year":"2006"},{"key":"10.1016\/j.ejmg.2008.06.004_bib6","doi-asserted-by":"crossref","first-page":"1046","DOI":"10.1016\/S0140-6736(71)91606-0","article-title":"Special pattern of widespread neuroblastoma with a favourable prognosis","volume":"1","author":"D'Angio","year":"1971","journal-title":"Lancet"},{"key":"10.1016\/j.ejmg.2008.06.004_bib7","doi-asserted-by":"crossref","first-page":"1265","DOI":"10.1200\/JCO.1998.16.4.1265","article-title":"Spontaneous regression of localized neuroblastoma detected by mass screening","volume":"16","author":"Yamamoto","year":"1998","journal-title":"J. Clin. Oncol."},{"key":"10.1016\/j.ejmg.2008.06.004_bib8","doi-asserted-by":"crossref","first-page":"225","DOI":"10.1056\/NEJM199601253340404","article-title":"Allelic loss of chromosome 1p as a predictor of unfavorable outcome in patients with neuroblastoma","volume":"334","author":"Caron","year":"1996","journal-title":"N. Engl. J. Med."},{"key":"10.1016\/j.ejmg.2008.06.004_bib9","doi-asserted-by":"crossref","first-page":"803","DOI":"10.1038\/sj.onc.1210675","article-title":"Expression and sequence analysis of candidates for the 1p36.31 tumor suppressor gene deleted in neuroblastomas","volume":"27","author":"Okawa","year":"2008","journal-title":"Oncogene"},{"key":"10.1016\/j.ejmg.2008.06.004_bib10","doi-asserted-by":"crossref","first-page":"459","DOI":"10.1016\/j.cell.2006.11.052","article-title":"CHD5 is a tumor suppressor at human 1p36","volume":"128","author":"Bagchi","year":"2007","journal-title":"Cell"}],"container-title":["European Journal of Medical Genetics"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S176972120800075X?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S176972120800075X?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,10,29]],"date-time":"2025-10-29T03:35:55Z","timestamp":1761708955000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S176972120800075X"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2008,11]]},"references-count":10,"journal-issue":{"issue":"6","published-print":{"date-parts":[[2008,11]]}},"alternative-id":["S176972120800075X"],"URL":"https:\/\/doi.org\/10.1016\/j.ejmg.2008.06.004","relation":{},"ISSN":["1769-7212"],"issn-type":[{"type":"print","value":"1769-7212"}],"subject":[],"published":{"date-parts":[[2008,11]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Complex constitutional subtelomeric 1p36.3 deletion\/duplication in a mentally retarded child with neonatal neuroblastoma","name":"articletitle","label":"Article Title"},{"value":"European Journal of Medical Genetics","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.ejmg.2008.06.004","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"Copyright \u00a9 2008 Elsevier Masson SAS. All rights reserved.","name":"copyright","label":"Copyright"}]}}