{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,12,19]],"date-time":"2025-12-19T09:42:13Z","timestamp":1766137333280,"version":"build-2065373602"},"reference-count":7,"publisher":"Elsevier BV","issue":"1","license":[{"start":{"date-parts":[[2020,1,1]],"date-time":"2020-01-01T00:00:00Z","timestamp":1577836800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2020,1,1]],"date-time":"2020-01-01T00:00:00Z","timestamp":1577836800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2019,11,9]],"date-time":"2019-11-09T00:00:00Z","timestamp":1573257600000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"funder":[{"DOI":"10.13039\/501100004663","name":"Ministry of Science and Technology, Taiwan","doi-asserted-by":"publisher","award":["107-2314-B-371-009-MY3"],"award-info":[{"award-number":["107-2314-B-371-009-MY3"]}],"id":[{"id":"10.13039\/501100004663","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["clinicalkey.com","clinicalkey.com.au","clinicalkey.es","clinicalkey.jp","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Taiwanese Journal of Obstetrics and Gynecology"],"published-print":{"date-parts":[[2020,1]]},"DOI":"10.1016\/j.tjog.2019.11.027","type":"journal-article","created":{"date-parts":[[2020,1,22]],"date-time":"2020-01-22T10:31:57Z","timestamp":1579689117000},"page":"157-161","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":4,"title":["Prenatal diagnosis of partial monosomy 21q (21q22.1\u2192qter) associated with intrauterine growth restriction and corpus callosum dysgenesis"],"prefix":"10.1016","volume":"59","author":[{"given":"Ying-Chung","family":"Chen","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Wan-Ju","family":"Wu","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Shun-Ping","family":"Chang","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Gwo-Chin","family":"Ma","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ming","family":"Chen","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.tjog.2019.11.027_bib1","first-page":"965401","article-title":"Monosomy 21 seen in live born is unlikely to represent true monosomy 21: a case report and review of the literature","volume":"2014","author":"Burgess","year":"2014","journal-title":"Case Rep Genet"},{"key":"10.1016\/j.tjog.2019.11.027_bib2","doi-asserted-by":"crossref","first-page":"454","DOI":"10.1038\/ejhg.2008.214","article-title":"Genotype-phenotype correlations in Down syndrome identified by array CGH in 30 cases of partial trisomy and partial monosomy chromosome 21","volume":"17","author":"Lyle","year":"2009","journal-title":"Eur J Hum Genet"},{"key":"10.1016\/j.tjog.2019.11.027_bib3","doi-asserted-by":"crossref","first-page":"235","DOI":"10.1038\/ejhg.2010.150","article-title":"Genomic analysis of partial 21q monosomies with variable phenotypes","volume":"19","author":"Roberson","year":"2011","journal-title":"Eur J Hum Genet"},{"key":"10.1016\/j.tjog.2019.11.027_bib4","doi-asserted-by":"crossref","first-page":"21","DOI":"10.1186\/s13039-016-0230-3","article-title":"Dissection of partial 21q monosomy in different phenotypes: clinical and molecular characterization of five cases and review of the literature","volume":"9","author":"Errichiello","year":"2016","journal-title":"Mol Cytogenet"},{"key":"10.1016\/j.tjog.2019.11.027_bib5","doi-asserted-by":"crossref","first-page":"69","DOI":"10.1002\/ajmg.a.20622","article-title":"A\u00a0prenatally diagnosed patient with full monosomy 21: ultrasound, cytogenetic, clinical, molecular, and necropsy findings","volume":"127A","author":"Mori","year":"2004","journal-title":"Am J Med Genet A"},{"key":"10.1016\/j.tjog.2019.11.027_bib6","doi-asserted-by":"crossref","first-page":"379","DOI":"10.1097\/AOG.0000000000000400","article-title":"Noninvasive prenatal testing for microdeletion syndromes and expanded trisomies: proceed with caution","volume":"124","author":"Bombard","year":"2014","journal-title":"Obstet Gynecol"},{"key":"10.1016\/j.tjog.2019.11.027_bib7","doi-asserted-by":"crossref","first-page":"25","DOI":"10.1002\/uog.13377","article-title":"Genome-wide normalized score: a novel algorithm to detect fetal trisomy 21 during non-invasive prenatal testing","volume":"44","author":"Yeang","year":"2014","journal-title":"Ultrasound Obstet Gynecol"}],"container-title":["Taiwanese Journal of Obstetrics and Gynecology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1028455919302943?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1028455919302943?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,10,19]],"date-time":"2025-10-19T18:16:59Z","timestamp":1760897819000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S1028455919302943"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2020,1]]},"references-count":7,"journal-issue":{"issue":"1","published-print":{"date-parts":[[2020,1]]}},"alternative-id":["S1028455919302943"],"URL":"https:\/\/doi.org\/10.1016\/j.tjog.2019.11.027","relation":{},"ISSN":["1028-4559"],"issn-type":[{"type":"print","value":"1028-4559"}],"subject":[],"published":{"date-parts":[[2020,1]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Prenatal diagnosis of partial monosomy 21q (21q22.1\u2192qter) associated with intrauterine growth restriction and corpus callosum dysgenesis","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.2019.11.027","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2020 Taiwan Association of Obstetrics & Gynecology. Publishing services by Elsevier B.V.","name":"copyright","label":"Copyright"}]}}