{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,3]],"date-time":"2026-10-03T23:04:32Z","timestamp":1791068672542,"version":"4.1.0"},"reference-count":6,"publisher":"Elsevier BV","issue":"3","license":[{"start":{"date-parts":[[2024,5,1]],"date-time":"2024-05-01T00:00:00Z","timestamp":1714521600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2024,5,1]],"date-time":"2024-05-01T00:00:00Z","timestamp":1714521600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2024,3,26]],"date-time":"2024-03-26T00:00:00Z","timestamp":1711411200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"funder":[{"DOI":"10.13039\/100020595","name":"National Science and Technology Council","doi-asserted-by":"publisher","id":[{"id":"10.13039\/100020595","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["clinicalkey.jp","clinicalkey.es","clinicalkey.com.au","clinicalkey.com","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Taiwanese Journal of Obstetrics and Gynecology"],"published-print":{"date-parts":[[2024,5]]},"DOI":"10.1016\/j.tjog.2024.03.012","type":"journal-article","created":{"date-parts":[[2024,5,25]],"date-time":"2024-05-25T15:38:17Z","timestamp":1716651497000},"page":"426-427","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":2,"title":["Prenatal diagnosis of familial 17q11.2 duplication encompassing NF1 in a pregnancy associated with asymptomatic carrier parent"],"prefix":"10.1016","volume":"63","author":[{"given":"Chih-Ping","family":"Chen","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1016\/j.tjog.2024.03.012_bib1","doi-asserted-by":"crossref","DOI":"10.1371\/journal.pone.0000327","article-title":"Clinical implementation of chromosomal microarray analysis: summary of 2513 postnatal cases","volume":"2","author":"Lu","year":"2007","journal-title":"PLoS One"},{"key":"10.1016\/j.tjog.2024.03.012_bib2","doi-asserted-by":"crossref","first-page":"305","DOI":"10.1038\/sj.ejhg.5201978","article-title":"NF1 microduplication first clinical report: association with mild mental retardation, early onset of baldness and dental enamel hypoplasia?","volume":"16","author":"Grisart","year":"2008","journal-title":"Eur J Hum Genet"},{"key":"10.1016\/j.tjog.2024.03.012_bib3","doi-asserted-by":"crossref","first-page":"508","DOI":"10.1038\/gim.2011.46","article-title":"NF1 microduplications: identification of seven nonrelated individuals provides further characterization of the phenotype","volume":"14","author":"Moles","year":"2012","journal-title":"Genet Med"},{"key":"10.1016\/j.tjog.2024.03.012_bib4","doi-asserted-by":"crossref","first-page":"303","DOI":"10.1136\/adc.42.223.303","article-title":"Pulmonary stenosis, caf\u00e9-au-lait spots, and dull intelligence","volume":"42","author":"Watson","year":"1967","journal-title":"Arch Dis Child"},{"key":"10.1016\/j.tjog.2024.03.012_bib5","first-page":"105","article-title":"Pulmonary stenosis, cafe au lait spots and dull intelligence: the Watson syndrome revisited","volume":"4","author":"Partington","year":"1985","journal-title":"(Abstract) Proc Greenwood Genet Center"},{"key":"10.1016\/j.tjog.2024.03.012_bib6","doi-asserted-by":"crossref","first-page":"752","DOI":"10.1136\/jmg.28.11.752","article-title":"Watson syndrome: is it a subtype of type 1 neurofibromatosis?","volume":"28","author":"Allanson","year":"1991","journal-title":"J\u00a0Med Genet"}],"container-title":["Taiwanese Journal of Obstetrics and Gynecology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1028455924000895?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1028455924000895?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2024,5,25]],"date-time":"2024-05-25T15:38:21Z","timestamp":1716651501000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S1028455924000895"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2024,5]]},"references-count":6,"journal-issue":{"issue":"3","published-print":{"date-parts":[[2024,5]]}},"alternative-id":["S1028455924000895"],"URL":"https:\/\/doi.org\/10.1016\/j.tjog.2024.03.012","relation":{},"ISSN":["1028-4559"],"issn-type":[{"value":"1028-4559","type":"print"}],"subject":[],"published":{"date-parts":[[2024,5]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Prenatal diagnosis of familial 17q11.2 duplication encompassing NF1 in a pregnancy associated with asymptomatic carrier parent","name":"articletitle","label":"Article Title"},{"value":"Taiwanese Journal of Obstetrics and Gynecology","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.tjog.2024.03.012","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2024 Taiwan Association of Obstetrics & Gynecology. Publishing services by Elsevier B.V.","name":"copyright","label":"Copyright"}]}}