{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,30]],"date-time":"2026-10-30T02:08:45Z","timestamp":1793326125200,"version":"4.5.0"},"reference-count":17,"publisher":"Elsevier BV","issue":"3","license":[{"start":{"date-parts":[[2023,5,1]],"date-time":"2023-05-01T00:00:00Z","timestamp":1682899200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2023,5,1]],"date-time":"2023-05-01T00:00:00Z","timestamp":1682899200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2023,3,18]],"date-time":"2023-03-18T00:00:00Z","timestamp":1679097600000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"funder":[{"DOI":"10.13039\/501100004861","name":"Mackay Memorial Hospital","doi-asserted-by":"publisher","id":[{"id":"10.13039\/501100004861","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/501100004663","name":"Ministry of Science and Technology, Taiwan","doi-asserted-by":"publisher","award":["MMH-E-111-04"],"award-info":[{"award-number":["MMH-E-111-04"]}],"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":[[2023,5]]},"DOI":"10.1016\/j.tjog.2023.03.010","type":"journal-article","created":{"date-parts":[[2023,5,15]],"date-time":"2023-05-15T08:55:02Z","timestamp":1684140902000},"page":"466-469","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":6,"title":["Low-level mosaic trisomy 20 without uniparental disomy 20\u00a0at amniocentesis in a pregnancy associated with a favorable outcome, cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes and perinatal progressive decrease of the aneuploid cell line"],"prefix":"10.1016","volume":"62","author":[{"given":"Chih-Ping","family":"Chen","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Fang-Tzu","family":"Wu","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yen-Ting","family":"Pan","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Schu-Rern","family":"Chern","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Peih-Shan","family":"Wu","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Chen-Chi","family":"Lee","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Wayseen","family":"Wang","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1016\/j.tjog.2023.03.010_bib1","doi-asserted-by":"crossref","first-page":"581","DOI":"10.1002\/pd.1970070809","article-title":"Trisomy 20 mosaicism in prenatal diagnosis - a review and update","volume":"7","author":"Hsu","year":"1987","journal-title":"Prenat Diagn"},{"key":"10.1016\/j.tjog.2023.03.010_bib2","doi-asserted-by":"crossref","first-page":"145","DOI":"10.1016\/j.tjog.2013.01.021","article-title":"Discrepancy in the trisomy mosaicism level between cultured amniocytes and uncultured amniocytes in prenatally detected mosaic trisomy 20","volume":"52","author":"Chen","year":"2013","journal-title":"Taiwan J Obstet Gynecol"},{"key":"10.1016\/j.tjog.2023.03.010_bib3","doi-asserted-by":"crossref","first-page":"146","DOI":"10.1016\/j.tjog.2019.11.024","article-title":"Cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes in mosaic double trisomy involving trisomy 7 and trisomy 20 (48,XY,+7,+20) at amniocentesis","volume":"59","author":"Chen","year":"2020","journal-title":"Taiwan J Obstet Gynecol"},{"key":"10.1016\/j.tjog.2023.03.010_bib4","doi-asserted-by":"crossref","first-page":"327","DOI":"10.1016\/j.tjog.2020.01.026","article-title":"Prenatal diagnosis of low-level mosaic trisomy 20 by amniocentesis in a pregnancy with a favorable outcome","volume":"59","author":"Chen","year":"2020","journal-title":"Taiwan J Obstet Gynecol"},{"key":"10.1016\/j.tjog.2023.03.010_bib5","doi-asserted-by":"crossref","first-page":"138","DOI":"10.1016\/j.tjog.2021.11.023","article-title":"Cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes in mosaic trisomy 20 at amniocentesis in a pregnancy with a favorable outcome","volume":"61","author":"Chen","year":"2022","journal-title":"Taiwan J Obstet Gynecol"},{"key":"10.1016\/j.tjog.2023.03.010_bib6","doi-asserted-by":"crossref","first-page":"675","DOI":"10.1016\/j.tjog.2022.05.003","article-title":"Prenatal diagnosis of pseudomosaicism for trisomy 20 at amniocentesis with a negative non-invasive prenatal testing (NIPT) result in a pregnancy with a favorable outcome","volume":"61","author":"Chen","year":"2022","journal-title":"Taiwan J Obstet Gynecol"},{"key":"10.1016\/j.tjog.2023.03.010_bib7","doi-asserted-by":"crossref","first-page":"103","DOI":"10.1002\/(SICI)1097-0223(200002)20:2<103::AID-PD761>3.0.CO;2-K","article-title":"Common trisomy mosaicism diagnosed in amniocytes involving chromosomes 13, 18, 20 and 21: karyotype-phenotype correlations","volume":"20","author":"Wallerstein","year":"2000","journal-title":"Prenat Diagn"},{"key":"10.1016\/j.tjog.2023.03.010_bib8","doi-asserted-by":"crossref","first-page":"239","DOI":"10.1002\/pd.1121","article-title":"Prenatally detected trisomy 20 mosaicism","volume":"25","author":"Robinson","year":"2005","journal-title":"Prenat Diagn"},{"key":"10.1016\/j.tjog.2023.03.010_bib9","first-page":"773","article-title":"Mosaic trisomy 20: discrepancy between cyto-and molecular genetic technologies in prenatal diagnosis","volume":"39","author":"Jin","year":"2022","journal-title":"Zhonghua Yi Xue Yi Chuan Xue Za Zhi"},{"key":"10.1016\/j.tjog.2023.03.010_bib10","doi-asserted-by":"crossref","first-page":"210","DOI":"10.1016\/j.tjog.2022.02.006","article-title":"Prenatal diagnosis and genetic counseling of uniparental disomy","volume":"61","author":"Chien","year":"2022","journal-title":"Taiwan J Obstet Gynecol"},{"key":"10.1016\/j.tjog.2023.03.010_bib11","doi-asserted-by":"crossref","first-page":"533","DOI":"10.1038\/sj.ejhg.5200287","article-title":"Maternal UPD 20 in a hyperactive child with severe growth retardation","volume":"7","author":"Chudoba","year":"1999","journal-title":"Eur J Hum Genet"},{"key":"10.1016\/j.tjog.2023.03.010_bib12","doi-asserted-by":"crossref","first-page":"86","DOI":"10.1136\/jmg.38.2.86","article-title":"Identification of interstitial maternal uniparental disomy (UPD) (14) and complete maternal UPD(20) in a cohort of growth retarded patients","volume":"38","author":"Eggermann","year":"2001","journal-title":"J\u00a0Med Genet"},{"key":"10.1016\/j.tjog.2023.03.010_bib13","doi-asserted-by":"crossref","first-page":"860","DOI":"10.1002\/pd.158","article-title":"Maternal UPD 20 in an infant from a pregnancy with mosaic trisomy 20","volume":"21","author":"Salafsky","year":"2001","journal-title":"Prenat Diagn"},{"key":"10.1016\/j.tjog.2023.03.010_bib14","doi-asserted-by":"crossref","first-page":"694","DOI":"10.1038\/sj.ejhg.5200867","article-title":"Maternal uniparental isodisomy 20 in a foetus with trisomy 20 mosaicism: clinical, cytogenetic and molecular analysis","volume":"10","author":"Velissariou","year":"2002","journal-title":"Eur J Hum Genet"},{"key":"10.1016\/j.tjog.2023.03.010_bib15","doi-asserted-by":"crossref","first-page":"309","DOI":"10.1038\/gim.2015.103","article-title":"Maternal uniparental disomy of chromosome 20: a novel imprinting disorder of growth failure","volume":"18","author":"Mulchandani","year":"2016","journal-title":"Genet Med"},{"key":"10.1016\/j.tjog.2023.03.010_bib16","doi-asserted-by":"crossref","first-page":"2083","DOI":"10.1210\/jc.2017-02780","article-title":"Maternal uniparental disomy for chromosome 20: physical and endocrinological characteristics of five patients","volume":"103","author":"Kawashima","year":"2018","journal-title":"J\u00a0Clin Endocrinol Metab"},{"key":"10.1016\/j.tjog.2023.03.010_bib17","doi-asserted-by":"crossref","first-page":"902","DOI":"10.1111\/cge.13727","article-title":"upd(20)mat is a rare cause of the Silver-Russell-syndrome-like phenotype: two unrelated cases and screening of large cohorts","volume":"97","author":"Hjortsh\u00f8j","year":"2020","journal-title":"Clin Genet"}],"container-title":["Taiwanese Journal of Obstetrics and Gynecology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1028455923000876?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1028455923000876?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,10,19]],"date-time":"2025-10-19T18:21:51Z","timestamp":1760898111000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S1028455923000876"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2023,5]]},"references-count":17,"journal-issue":{"issue":"3","published-print":{"date-parts":[[2023,5]]}},"alternative-id":["S1028455923000876"],"URL":"https:\/\/doi.org\/10.1016\/j.tjog.2023.03.010","relation":{},"ISSN":["1028-4559"],"issn-type":[{"value":"1028-4559","type":"print"}],"subject":[],"published":{"date-parts":[[2023,5]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Low-level mosaic trisomy 20 without uniparental disomy 20\u00a0at amniocentesis in a pregnancy associated with a favorable outcome, cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes and perinatal progressive decrease of the aneuploid cell line","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.2023.03.010","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2023 Taiwan Association of Obstetrics & Gynecology. Publishing services by Elsevier B.V.","name":"copyright","label":"Copyright"}]}}