{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,1,9]],"date-time":"2025-01-09T05:26:15Z","timestamp":1736400375225,"version":"3.32.0"},"reference-count":5,"publisher":"Elsevier BV","issue":"1","license":[{"start":{"date-parts":[[2025,1,1]],"date-time":"2025-01-01T00:00:00Z","timestamp":1735689600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2025,1,1]],"date-time":"2025-01-01T00:00:00Z","timestamp":1735689600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2024,11,5]],"date-time":"2024-11-05T00:00:00Z","timestamp":1730764800000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"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":[[2025,1]]},"DOI":"10.1016\/j.tjog.2024.10.009","type":"journal-article","created":{"date-parts":[[2025,1,8]],"date-time":"2025-01-08T15:46:24Z","timestamp":1736351184000},"page":"182-183","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":0,"title":["Prenatal diagnosis and genetic counselling of a rare maternal inherited chromosome 1q21.1q21.2 microduplication with no phenotypic abnormalities"],"prefix":"10.1016","volume":"64","author":[{"given":"Mingxia","family":"Xie","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Xinfang","family":"He","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Tou","family":"Tou","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ruixue","family":"Liu","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.tjog.2024.10.009_bib1","doi-asserted-by":"crossref","first-page":"319","DOI":"10.1002\/ajmg.a.38564","article-title":"Incomplete penetrance, variable expressivity, or dosage insensitivity in four families with directly transmitted unbalanced chromosome abnormalities","volume":"176","author":"Bateman","year":"2018","journal-title":"Am J Med Genet"},{"issue":"1","key":"10.1016\/j.tjog.2024.10.009_bib2","doi-asserted-by":"crossref","first-page":"197","DOI":"10.1186\/s12920-023-01618-4","article-title":"Genetic and ultrasonographic analyses of fetuses with 1q21.1q21.2 microdeletion\/microduplication: a retrospective study","volume":"16","author":"Guo","year":"2023","journal-title":"BMC Med Genom"},{"key":"10.1016\/j.tjog.2024.10.009_bib3","doi-asserted-by":"crossref","DOI":"10.1155\/2013\/346762","article-title":"Implementation of high resolution whole genome array CGH in the prenatal clinical setting: advantages, challenges, and review of the literature","volume":"2013","author":"Evangelidou","year":"2013","journal-title":"BioMed Res Int"},{"issue":"4","key":"10.1016\/j.tjog.2024.10.009_bib4","doi-asserted-by":"crossref","DOI":"10.1002\/jgm.2948","article-title":"Clinical and molecular cytogenetic analyses of four families with 1q21.1 microdeletion or microduplication","volume":"19","author":"Wang","year":"2017","journal-title":"J\u00a0Gene Med"},{"key":"10.1016\/j.tjog.2024.10.009_bib5","doi-asserted-by":"crossref","first-page":"163","DOI":"10.3389\/fped.2018.00163","article-title":"Narrowing the genetic causes of language dysfunction in the 1q21.1 microduplication syndrome","volume":"6","author":"Antonio","year":"2018","journal-title":"Front Pediatr"}],"container-title":["Taiwanese Journal of Obstetrics and Gynecology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1028455924003036?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1028455924003036?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,1,8]],"date-time":"2025-01-08T15:46:26Z","timestamp":1736351186000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S1028455924003036"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2025,1]]},"references-count":5,"journal-issue":{"issue":"1","published-print":{"date-parts":[[2025,1]]}},"alternative-id":["S1028455924003036"],"URL":"https:\/\/doi.org\/10.1016\/j.tjog.2024.10.009","relation":{},"ISSN":["1028-4559"],"issn-type":[{"value":"1028-4559","type":"print"}],"subject":[],"published":{"date-parts":[[2025,1]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Prenatal diagnosis and genetic counselling of a rare maternal inherited chromosome 1q21.1q21.2 microduplication with no phenotypic abnormalities","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.2024.10.009","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\u00e9","name":"copyright","label":"Copyright"}]}}