{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,27]],"date-time":"2026-05-27T17:29:26Z","timestamp":1779902966505,"version":"3.53.1"},"reference-count":12,"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\/100020595","name":"National Science and Technology Council","doi-asserted-by":"publisher","award":["MMH-E-111-04"],"award-info":[{"award-number":["MMH-E-111-04"]}],"id":[{"id":"10.13039\/100020595","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.2023.03.006","type":"journal-article","created":{"date-parts":[[2023,5,15]],"date-time":"2023-05-15T08:54:41Z","timestamp":1684140881000},"page":"444-447","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":4,"title":["Prenatal diagnosis and molecular genetic analysis of recurrent trisomy 18 of maternal origin in two consecutive pregnancies"],"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":"Chian-Huey","family":"Wong","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Shin-Wen","family":"Chen","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Schu-Rern","family":"Chern","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yen-Ting","family":"Pan","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Wen-Lin","family":"Chen","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.2023.03.006_bib1","doi-asserted-by":"crossref","first-page":"194","DOI":"10.1016\/j.tjog.2015.01.001","article-title":"First-trimester diagnosis of recurrent omphalocele associated with fetal trisomy 18 but without parental mosaicism","volume":"54","author":"Chen","year":"2015","journal-title":"Taiwan J Obstet Gynecol"},{"key":"10.1016\/j.tjog.2023.03.006_bib2","doi-asserted-by":"crossref","first-page":"373","DOI":"10.1111\/j.1447-0756.1999.tb01180.x","article-title":"Risk of recurrence of fetal chromosomal aberrations: analysis of trisomy 21, trisomy 18, trisomy 13, and 45,X in 1,076 Japanese mothers","volume":"25","author":"Uehara","year":"1999","journal-title":"J\u00a0Obstet Gynaecol Res"},{"key":"10.1016\/j.tjog.2023.03.006_bib3","doi-asserted-by":"crossref","first-page":"81","DOI":"10.1186\/1750-1172-7-81","article-title":"The trisomy 18 syndrome","volume":"7","author":"Cereda","year":"2012","journal-title":"Orphanet J Rare Dis"},{"key":"10.1016\/j.tjog.2023.03.006_bib4","doi-asserted-by":"crossref","first-page":"287","DOI":"10.12891\/ceog2084.2016","article-title":"A\u00a0rare occurrence of three consecutive autosomal trisomic pregnancies in a couple without offspring","volume":"43","author":"Burada","year":"2016","journal-title":"Clin Exp Obstet Gynecol"},{"key":"10.1016\/j.tjog.2023.03.006_bib5","doi-asserted-by":"crossref","first-page":"869","DOI":"10.1139\/g72-106","article-title":"Stability of trisomic [47, 18+] cells in long-term mosaic skin fibroblast culture","volume":"15","author":"Beratis","year":"1972","journal-title":"Can J Genet Cytol"},{"key":"10.1016\/j.tjog.2023.03.006_bib6","doi-asserted-by":"crossref","first-page":"298","DOI":"10.1007\/BF00200581","article-title":"Trisomy 18 mosaicism in an adult woman with normal intelligence and history of miscarriage","volume":"84","author":"Gersdorf","year":"1990","journal-title":"Hum Genet"},{"key":"10.1016\/j.tjog.2023.03.006_bib7","doi-asserted-by":"crossref","first-page":"240","DOI":"10.1002\/(SICI)1096-8628(19970120)68:2<240::AID-AJMG24>3.0.CO;2-T","article-title":"Trisomy 18 mosaicism in a woman with normal intelligence, pigmentary dysplasia, and an 18 trisomic daughter","volume":"68","author":"Ukita","year":"1997","journal-title":"Am J Med Genet"},{"key":"10.1016\/j.tjog.2023.03.006_bib8","doi-asserted-by":"crossref","first-page":"303","DOI":"10.1002\/ajmg.a.20213","article-title":"Trisomy 18 mosaicism in a woman with normal intelligence","volume":"120A","author":"Bettio","year":"2003","journal-title":"Am J Med Genet"},{"key":"10.1016\/j.tjog.2023.03.006_bib9","doi-asserted-by":"crossref","first-page":"505","DOI":"10.1002\/ajmg.a.31535","article-title":"Phenotypic spectrum of mosaic trisomy 18: two new patients, review of the literature and counseling issues","volume":"143A","author":"Tucker","year":"2007","journal-title":"Am J Med Genet"},{"key":"10.1016\/j.tjog.2023.03.006_bib10","doi-asserted-by":"crossref","first-page":"902","DOI":"10.1016\/j.tjog.2016.10.001","article-title":"Prenatal diagnosis of low-level mosaicism for trisomy 18 associated with a favorable fetal outcome","volume":"55","author":"Chen","year":"2016","journal-title":"Taiwan J Obstet Gynecol"},{"key":"10.1016\/j.tjog.2023.03.006_bib11","doi-asserted-by":"crossref","first-page":"684","DOI":"10.1016\/j.tjog.2022.05.005","article-title":"Cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes in mosaic trisomy 18 at amniocentesis in a pregnancy with a favorable fetal outcome and maternal uniparental disomy 18","volume":"61","author":"Chen","year":"2022","journal-title":"Taiwan J Obstet Gynecol"},{"key":"10.1016\/j.tjog.2023.03.006_bib12","doi-asserted-by":"crossref","first-page":"690","DOI":"10.1016\/j.tjog.2022.05.006","article-title":"Mosaic trisomy 18 at amniocentesis associated with a favorable fetal outcome in a pregnancy","volume":"61","author":"Chen","year":"2022","journal-title":"Taiwan J Obstet Gynecol"}],"container-title":["Taiwanese Journal of Obstetrics and Gynecology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1028455923000827?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1028455923000827?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,10,19]],"date-time":"2025-10-19T18:21:47Z","timestamp":1760898107000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S1028455923000827"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2023,5]]},"references-count":12,"journal-issue":{"issue":"3","published-print":{"date-parts":[[2023,5]]}},"alternative-id":["S1028455923000827"],"URL":"https:\/\/doi.org\/10.1016\/j.tjog.2023.03.006","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":"Prenatal diagnosis and molecular genetic analysis of recurrent trisomy 18 of maternal origin in two consecutive pregnancies","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.2023.03.006","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"}]}}