{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,3,18]],"date-time":"2026-03-18T01:22:43Z","timestamp":1773796963532,"version":"3.50.1"},"reference-count":6,"publisher":"Elsevier BV","issue":"2","license":[{"start":{"date-parts":[[2025,3,1]],"date-time":"2025-03-01T00:00:00Z","timestamp":1740787200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2025,3,1]],"date-time":"2025-03-01T00:00:00Z","timestamp":1740787200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2025,1,15]],"date-time":"2025-01-15T00:00:00Z","timestamp":1736899200000},"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":[[2025,3]]},"DOI":"10.1016\/j.tjog.2024.12.013","type":"journal-article","created":{"date-parts":[[2025,3,4]],"date-time":"2025-03-04T15:55:00Z","timestamp":1741103700000},"page":"345-347","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":1,"title":["Prenatal diagnosis of a de novo 17q25.3 microdeletion encompassing RAC3 and CSNK1D in a fetus associated with partial agenesis of the corpus callosum, small brain volume, micrognathia and total anomalous pulmonary venous return"],"prefix":"10.1016","volume":"64","author":[{"given":"Chih-Ping","family":"Chen","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Liang-Kai","family":"Wang","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Fang-Tzu","family":"Wu","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Yen-Ting","family":"Pan","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Peih-Shan","family":"Wu","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Wayseen","family":"Wang","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.tjog.2024.12.013_bib1","doi-asserted-by":"crossref","first-page":"75","DOI":"10.1186\/s13023-015-0291-0","article-title":"De novo deletions and duplications of 17q25.3 cause susceptibility to cardiovascular malformations","volume":"10","author":"Probst","year":"2015","journal-title":"Orphanet J Rare Dis"},{"key":"10.1016\/j.tjog.2024.12.013_bib2","doi-asserted-by":"crossref","first-page":"27","DOI":"10.1016\/j.ajhg.2017.10.002","article-title":"WNT signaling perturbations underlie the genetic heterogeneity of Robinow syndrome","volume":"102","author":"White","year":"2018","journal-title":"Am J Hum Genet"},{"key":"10.1016\/j.tjog.2024.12.013_bib3","doi-asserted-by":"crossref","first-page":"1021","DOI":"10.1038\/s41436-018-0323-y","article-title":"De novo missense variants in RAC3 cause a novel neurodevelopmental syndrome","volume":"21","author":"Costain","year":"2019","journal-title":"Genet Med"},{"key":"10.1016\/j.tjog.2024.12.013_bib4","doi-asserted-by":"crossref","first-page":"3308","DOI":"10.1093\/brain\/awac106","article-title":"Variant-specific changes in RAC3 function disrupt corticogenesis in neurodevelopmental phenotypes","volume":"145","author":"Scala","year":"2022","journal-title":"Brain"},{"key":"10.1016\/j.tjog.2024.12.013_bib5","doi-asserted-by":"crossref","first-page":"478","DOI":"10.1002\/pd.6106","article-title":"Prenatal imaging features related to RAC3 pathogenic variant and differential diagnoses","volume":"42","author":"Cabet","year":"2022","journal-title":"Prenat Diagn"},{"key":"10.1016\/j.tjog.2024.12.013_bib6","doi-asserted-by":"crossref","first-page":"1597","DOI":"10.1007\/s00381-024-06285-z","article-title":"An unusual presentation of de novo RAC3 variation in prenatal diagnosis","volume":"40","author":"Meunier","year":"2024","journal-title":"Childs Nerv Syst"}],"container-title":["Taiwanese Journal of Obstetrics and Gynecology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1028455925000361?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1028455925000361?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,3,10]],"date-time":"2025-03-10T15:38:26Z","timestamp":1741621106000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S1028455925000361"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2025,3]]},"references-count":6,"journal-issue":{"issue":"2","published-print":{"date-parts":[[2025,3]]}},"alternative-id":["S1028455925000361"],"URL":"https:\/\/doi.org\/10.1016\/j.tjog.2024.12.013","relation":{},"ISSN":["1028-4559"],"issn-type":[{"value":"1028-4559","type":"print"}],"subject":[],"published":{"date-parts":[[2025,3]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Prenatal diagnosis of a de novo 17q25.3 microdeletion encompassing RAC3 and CSNK1D in a fetus associated with partial agenesis of the corpus callosum, small brain volume, micrognathia and total anomalous pulmonary venous return","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.2024.12.013","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2025 Taiwan Association of Obstetrics & Gynecology. Publishing services by Elsevier B.V\u00e9","name":"copyright","label":"Copyright"}]}}