{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,19]],"date-time":"2025-10-19T20:50:36Z","timestamp":1760907036705,"version":"build-2065373602"},"reference-count":21,"publisher":"Elsevier BV","issue":"5","license":[{"start":{"date-parts":[[2019,9,1]],"date-time":"2019-09-01T00:00:00Z","timestamp":1567296000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2019,9,1]],"date-time":"2019-09-01T00:00:00Z","timestamp":1567296000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2019,7,9]],"date-time":"2019-07-09T00:00:00Z","timestamp":1562630400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"funder":[{"DOI":"10.13039\/100012553","name":"Chang Gung Memorial Hospital","doi-asserted-by":"crossref","award":["CORPG3G0301"],"award-info":[{"award-number":["CORPG3G0301"]}],"id":[{"id":"10.13039\/100012553","id-type":"DOI","asserted-by":"crossref"}]}],"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":[[2019,9]]},"DOI":"10.1016\/j.tjog.2019.07.014","type":"journal-article","created":{"date-parts":[[2019,9,18]],"date-time":"2019-09-18T18:45:11Z","timestamp":1568832311000},"page":"662-666","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":4,"title":["Prenatally diagnosed de novo segmental amplification or deletion by microarray-based comparative genomic hybridization: A retrospective study"],"prefix":"10.1016","volume":"58","author":[{"given":"Hsiu-Huei","family":"Peng","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Chien-Hong","family":"Lee","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Sheng-Yuan","family":"Su","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Kuan-Ju","family":"Chen","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Yen-Chang","family":"Lee","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Shu-Han","family":"You","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Wen-Fang","family":"Lee","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Po-Jen","family":"Cheng","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"issue":"3","key":"10.1016\/j.tjog.2019.07.014_bib1","doi-asserted-by":"crossref","first-page":"249","DOI":"10.2217\/pme-2015-0003","article-title":"Chromosomal microarray in prenatal diagnosis: case studies and clinical challenges","volume":"13","author":"Karla Leavitt","year":"2016","journal-title":"Pers Med"},{"issue":"2","key":"10.1016\/j.tjog.2019.07.014_bib2","doi-asserted-by":"crossref","first-page":"201","DOI":"10.1016\/j.fertnstert.2018.01.005","article-title":"Prenatal diagnosis by chromosomal microarray analysis","volume":"109","author":"Levy","year":"2018","journal-title":"Fertil Steril"},{"issue":"13","key":"10.1016\/j.tjog.2019.07.014_bib3","doi-asserted-by":"crossref","first-page":"1269","DOI":"10.1002\/pd.4685","article-title":"Routine use of array comparative genomic hybridization (aCGH) as standard approach for prenatal diagnosis of chromosomal abnormalities. Clinical experience of 1763 prenatal cases","volume":"35","author":"Papoulidis","year":"2015","journal-title":"Prenat Diagn"},{"issue":"5","key":"10.1016\/j.tjog.2019.07.014_bib4","doi-asserted-by":"crossref","first-page":"614","DOI":"10.1111\/j.1471-0528.2012.03279.x","article-title":"Clinical utility of array comparative genomic hybridisation for prenatal diagnosis: a cohort study of 3171 pregnancies","volume":"119","author":"Lee","year":"2012","journal-title":"Bjog"},{"issue":"1","key":"10.1016\/j.tjog.2019.07.014_bib5","doi-asserted-by":"crossref","first-page":"54","DOI":"10.1186\/s13039-016-0267-3","article-title":"A\u00a0de novo duplication of chromosome 9q34.13-qter in a fetus with tetralogy of Fallot syndrome","volume":"9","author":"Liu","year":"2016","journal-title":"Mol Cytogenet"},{"key":"10.1016\/j.tjog.2019.07.014_bib6","first-page":"6","article-title":"A\u00a0prenatally ascertained de novo terminal deletion of chromosomal bands 1q43q44 associated with multiple congenital abnormalities in a female fetus","volume":"2015","author":"Sismani","year":"2015","journal-title":"Case Rep Genet"},{"issue":"1","key":"10.1016\/j.tjog.2019.07.014_bib7","doi-asserted-by":"crossref","first-page":"27","DOI":"10.1002\/uog.14695","article-title":"Array comparative genomic hybridization and fetal congenital heart defects: a systematic review and meta-analysis","volume":"45","author":"Jansen","year":"2015","journal-title":"Ultrasound Obstet Gynecol"},{"issue":"2","key":"10.1016\/j.tjog.2019.07.014_bib8","doi-asserted-by":"crossref","first-page":"68","DOI":"10.1097\/MCD.0000000000000075","article-title":"An interstitial de-novo microdeletion of 3q26.33q27.3 causing severe intrauterine growth retardation","volume":"24","author":"Bouman","year":"2015","journal-title":"Clin Dysmorphol"},{"issue":"1","key":"10.1016\/j.tjog.2019.07.014_bib9","doi-asserted-by":"crossref","first-page":"34","DOI":"10.1186\/s13052-018-0467-z","volume":"44","author":"Maini","year":"2018","journal-title":"Ital J Pediatr"},{"issue":"1","key":"10.1016\/j.tjog.2019.07.014_bib10","doi-asserted-by":"crossref","first-page":"16","DOI":"10.1002\/bdra.23458","article-title":"Array-based molecular karyotyping in fetal brain malformations: identification of novel candidate genes and chromosomal regions","volume":"106","author":"Krutzke","year":"2016","journal-title":"Birth Defects Res Part A Clin Mol Teratol"},{"issue":"S1","key":"10.1016\/j.tjog.2019.07.014_bib11","doi-asserted-by":"crossref","first-page":"313","DOI":"10.1002\/uog.18514","article-title":"EP13.07: pathological findings in the study of prenatal arrays by structural ultrasound anomalies","volume":"50","author":"Herrero","year":"2017","journal-title":"Ultrasound Obstet Gynecol"},{"issue":"04","key":"10.1016\/j.tjog.2019.07.014_bib12","doi-asserted-by":"crossref","first-page":"215","DOI":"10.1055\/s-0037-1602696","article-title":"Array characterization of prenatally diagnosed 15q26 microdeletion and 2q37.1 duplication: report of a new case with multicystic kidneys and review of the literature","volume":"06","author":"Kammoun","year":"2017","journal-title":"J\u00a0Pediatr Genet"},{"issue":"2","key":"10.1016\/j.tjog.2019.07.014_bib13","doi-asserted-by":"crossref","first-page":"194","DOI":"10.3109\/14767058.2016.1168394","article-title":"Submicroscopic chromosomal abnormalities in fetuses with increased nuchal translucency and normal karyotype","volume":"30","author":"Yang","year":"2017","journal-title":"J\u00a0Matern Fetal Neonatal Med: Off J Eur Assoc Perinat Med Fed Asia Oceania Perinat Soc Int Soc Perinat Obst"},{"key":"10.1016\/j.tjog.2019.07.014_bib14","doi-asserted-by":"crossref","DOI":"10.1038\/gim.2018.19","article-title":"Prenatal upper-limb mesomelia and 2q31.1 microdeletions affecting the regulatory genome","author":"Peron","year":"2018","journal-title":"Genet Med"},{"issue":"10","key":"10.1016\/j.tjog.2019.07.014_bib15","doi-asserted-by":"crossref","first-page":"1693","DOI":"10.1093\/ndt\/gfv465","article-title":"Prenatal diagnosis of fetal multicystic dysplastic kidney via high-resolution whole-genome array","volume":"31","author":"Fu","year":"2016","journal-title":"Nephrol Dial Transplant"},{"issue":"11","key":"10.1016\/j.tjog.2019.07.014_bib16","doi-asserted-by":"crossref","first-page":"2934","DOI":"10.1002\/ajmg.a.37848","article-title":"17q12 deletion and duplication syndrome in Denmark\u2014a clinical cohort of 38 patients and review of the literature","volume":"170","author":"Rasmussen","year":"2016","journal-title":"Am J Med Genet"},{"issue":"12","key":"10.1016\/j.tjog.2019.07.014_bib17","doi-asserted-by":"crossref","first-page":"1265","DOI":"10.1002\/pd.4690","article-title":"Fetal phenotype of 17q12 microdeletion syndrome: renal echogenicity and congenital diaphragmatic hernia in 2 cases","volume":"35","author":"Yap","year":"2015","journal-title":"Prenat Diagn"},{"issue":"7","key":"10.1016\/j.tjog.2019.07.014_bib18","doi-asserted-by":"crossref","first-page":"619","DOI":"10.1016\/j.jogc.2016.02.010","article-title":"Prenatal array comparative genomic hybridization in fetuses with structural cardiac anomalies","volume":"38","author":"Lazier","year":"2016","journal-title":"J\u00a0Obstet Gynaecol Can"},{"issue":"6","key":"10.1016\/j.tjog.2019.07.014_bib19","doi-asserted-by":"crossref","first-page":"268","DOI":"10.1159\/000443942","article-title":"Differing microdeletion sizes and breakpoints in chromosome 7q11.23 in Williams-Beuren syndrome detected by chromosomal microarray analysis","volume":"6","author":"Li","year":"2015","journal-title":"Mol Syndromology"},{"issue":"6","key":"10.1016\/j.tjog.2019.07.014_bib20","doi-asserted-by":"crossref","first-page":"324","DOI":"10.1016\/j.siny.2014.09.003","article-title":"Genetic causes of congenital diaphragmatic hernia","volume":"19","author":"Wynn","year":"2014","journal-title":"Semin Fetal Neonatal Med"},{"issue":"8","key":"10.1016\/j.tjog.2019.07.014_bib21","doi-asserted-by":"crossref","first-page":"955","DOI":"10.1242\/dmm.028365","article-title":"Congenital diaphragmatic hernias: from genes to mechanisms to therapies","volume":"10","author":"Kardon","year":"2017","journal-title":"Dis Models Mech"}],"container-title":["Taiwanese Journal of Obstetrics and Gynecology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S102845591930169X?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S102845591930169X?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,10,19]],"date-time":"2025-10-19T18:16:58Z","timestamp":1760897818000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S102845591930169X"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2019,9]]},"references-count":21,"journal-issue":{"issue":"5","published-print":{"date-parts":[[2019,9]]}},"alternative-id":["S102845591930169X"],"URL":"https:\/\/doi.org\/10.1016\/j.tjog.2019.07.014","relation":{},"ISSN":["1028-4559"],"issn-type":[{"type":"print","value":"1028-4559"}],"subject":[],"published":{"date-parts":[[2019,9]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Prenatally diagnosed de novo segmental amplification or deletion by microarray-based comparative genomic hybridization: A retrospective study","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.2019.07.014","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2019 Taiwan Association of Obstetrics & Gynecology. Publishing services by Elsevier B.V.","name":"copyright","label":"Copyright"}]}}