{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,27]],"date-time":"2025-10-27T11:02:50Z","timestamp":1761562970529,"version":"build-2065373602"},"reference-count":10,"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.2023.03.007","type":"journal-article","created":{"date-parts":[[2023,5,15]],"date-time":"2023-05-15T08:54:58Z","timestamp":1684140898000},"page":"453-456","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":1,"title":["Molecular cytogenetic characterization of del(X)(p22.33)mat and de novo dup(4)(q34.3q35.2) in a male fetus with multiple anomalies of facial dysmorphism, ventriculomegaly, congenital heart defects, short long bones and clinodactyly"],"prefix":"10.1016","volume":"62","author":[{"given":"Chih-Ping","family":"Chen","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jian-Pei","family":"Huang","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Yi-Yung","family":"Chen","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Shin-Wen","family":"Chen","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Schu-Rern","family":"Chern","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Peih-Shan","family":"Wu","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":"Wen-Lin","family":"Chen","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Chen-Wen","family":"Pan","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.2023.03.007_bib1","doi-asserted-by":"crossref","first-page":"705","DOI":"10.1016\/j.tjog.2016.05.009","article-title":"Molecular cytogenetic characterization of Xp22.32\u2192pter deletion and Xq26.3\u2192qter duplication in a male fetus associated with 46,Y,rec(X)dup(Xq)inv(X)(p22.3q26.3), a hypoplastic left heart, short stature and maternal X chromosome pericentric inversion","volume":"55","author":"Chen","year":"2016","journal-title":"Taiwan J Obstet Gynecol"},{"key":"10.1016\/j.tjog.2023.03.007_bib2","doi-asserted-by":"crossref","first-page":"264","DOI":"10.1016\/j.tjog.2017.01.006","article-title":"Molecular cytogenetic characterization and prenatal diagnosis of familial Xp22.33 microdeletion encompassing short stature homeobox gene in a male fetus with a favorable outcome","volume":"56","author":"Chen","year":"2017","journal-title":"Taiwan J Obstet Gynecol"},{"key":"10.1016\/j.tjog.2023.03.007_bib3","series-title":"GeneReviews\u00ae [Internet]","article-title":"SHOX deficiency disorders","author":"Binder","year":"2018"},{"key":"10.1016\/j.tjog.2023.03.007_bib4","doi-asserted-by":"crossref","DOI":"10.1038\/ncomms10822","article-title":"FAT1 mutations cause a glomerulotubular nephropathy","volume":"7","author":"Gee","year":"2016","journal-title":"Nat Commun"},{"key":"10.1016\/j.tjog.2023.03.007_bib5","doi-asserted-by":"crossref","DOI":"10.1111\/cge.14194","article-title":"De novo 4q35.2 duplication containing FAT1 is associated with autism spectrum disorder","author":"Hernando-Davalillo","year":"2022","journal-title":"Clin Genet"},{"key":"10.1016\/j.tjog.2023.03.007_bib6","doi-asserted-by":"crossref","DOI":"10.1097\/MD.0000000000013094","article-title":"Clinical, cytogenetic, and molecular findings in a fetus with ultrasonic multiple malformations, 4q duplication, and 7q deletion: a case report and literature review","volume":"97","author":"Yue","year":"2018","journal-title":"Medicine (Baltim)"},{"key":"10.1016\/j.tjog.2023.03.007_bib7","doi-asserted-by":"crossref","first-page":"26","DOI":"10.1186\/s13039-020-00492-4","article-title":"Partial trisomy 4q and monosomy 5p inherited from a maternal translocation t(4;5)(q33; p15) in three adverse pregnancies","volume":"13","author":"Zhang","year":"2020","journal-title":"Mol Cytogenet"},{"key":"10.1016\/j.tjog.2023.03.007_bib8","doi-asserted-by":"crossref","first-page":"3","DOI":"10.1002\/ajmg.1320010103","article-title":"Inverted tandem (\"mirror\") duplications in human chromosomes: -nv dup 8p, 4q, 22q","volume":"1","author":"Taylor","year":"1977","journal-title":"Am J Med Genet"},{"key":"10.1016\/j.tjog.2023.03.007_bib9","doi-asserted-by":"crossref","first-page":"122","DOI":"10.1002\/ajmg.a.10093","article-title":"Cytogenetic and molecular characterization of a de novo 4q24qter duplication and correlation to the associated phenotype","volume":"118A","author":"Rinaldi","year":"2003","journal-title":"Am J Med Genet"},{"key":"10.1016\/j.tjog.2023.03.007_bib10","doi-asserted-by":"crossref","first-page":"113","DOI":"10.5507\/bp.2006.016","article-title":"A\u00a0duplication dup(4)(q28q35.2) de novo in a newborn","volume":"150","author":"Cernakova","year":"2006","journal-title":"Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub"}],"container-title":["Taiwanese Journal of Obstetrics and Gynecology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1028455923000840?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1028455923000840?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,10,19]],"date-time":"2025-10-19T18:21:24Z","timestamp":1760898084000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S1028455923000840"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2023,5]]},"references-count":10,"journal-issue":{"issue":"3","published-print":{"date-parts":[[2023,5]]}},"alternative-id":["S1028455923000840"],"URL":"https:\/\/doi.org\/10.1016\/j.tjog.2023.03.007","relation":{},"ISSN":["1028-4559"],"issn-type":[{"type":"print","value":"1028-4559"}],"subject":[],"published":{"date-parts":[[2023,5]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Molecular cytogenetic characterization of del(X)(p22.33)mat and de novo dup(4)(q34.3q35.2) in a male fetus with multiple anomalies of facial dysmorphism, ventriculomegaly, congenital heart defects, short long bones and clinodactyly","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.2023.03.007","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"}]}}