{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,19]],"date-time":"2025-10-19T18:41:04Z","timestamp":1760899264803,"version":"build-2065373602"},"reference-count":15,"publisher":"Elsevier BV","issue":"3","license":[{"start":{"date-parts":[[2017,6,1]],"date-time":"2017-06-01T00:00:00Z","timestamp":1496275200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2017,6,1]],"date-time":"2017-06-01T00:00:00Z","timestamp":1496275200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2017,4,9]],"date-time":"2017-04-09T00:00:00Z","timestamp":1491696000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"funder":[{"DOI":"10.13039\/100007225","name":"Ministry of Science and Technology","doi-asserted-by":"publisher","award":["MOST-104-2314-B-195-009","MOST-105-2314-B-195-012"],"award-info":[{"award-number":["MOST-104-2314-B-195-009","MOST-105-2314-B-195-012"]}],"id":[{"id":"10.13039\/100007225","id-type":"DOI","asserted-by":"publisher"}]},{"name":"MacKay Memorial Hospital, Taipei, Taiwan","award":["MMH-E-105-04"],"award-info":[{"award-number":["MMH-E-105-04"]}]}],"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":[[2017,6]]},"DOI":"10.1016\/j.tjog.2017.04.024","type":"journal-article","created":{"date-parts":[[2017,6,7]],"date-time":"2017-06-07T15:39:09Z","timestamp":1496849949000},"page":"390-393","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":1,"title":["Molecular genetic characterization of a prenatally detected de novo interstitial deletion of chromosome 20p (20p12-p13) encompassing JAG1 and a literature review of prenatal diagnosis of Alagille syndrome"],"prefix":"10.1016","volume":"56","author":[{"given":"Chih-Ping","family":"Chen","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Chang-Sheng","family":"Yin","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Liang-Kai","family":"Wang","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Schu-Rern","family":"Chern","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Shin-Wen","family":"Chen","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Shih-Ting","family":"Lai","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Peih-Shan","family":"Wu","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Wen-Lin","family":"Chen","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.2017.04.024_bib1","series-title":"Gene reviews","article-title":"Alagille syndrome","author":"Spinner","year":"1993"},{"key":"10.1016\/j.tjog.2017.04.024_bib2","doi-asserted-by":"crossref","first-page":"75","DOI":"10.2147\/TACG.S86420","article-title":"Alagille syndrome: clinical perspectives","volume":"9","author":"Saleh","year":"2016","journal-title":"Appl Clin Genet"},{"key":"10.1016\/j.tjog.2017.04.024_bib3","doi-asserted-by":"crossref","first-page":"80","DOI":"10.1002\/(SICI)1096-8628(19970502)70:1<80::AID-AJMG15>3.0.CO;2-T","article-title":"Deletions of 20p12 in Alagille syndrome: frequency and molecular characterization","volume":"70","author":"Krantz","year":"1997","journal-title":"Am J Med Genet"},{"key":"10.1016\/j.tjog.2017.04.024_bib4","doi-asserted-by":"crossref","first-page":"156","DOI":"10.1016\/j.febslet.2004.08.022","article-title":"Exon 6 of human Jagged-1 encodes an autonomously folding unit","volume":"574","author":"Guarnaccia","year":"2004","journal-title":"FEBS Lett"},{"key":"10.1016\/j.tjog.2017.04.024_bib5","doi-asserted-by":"crossref","first-page":"249","DOI":"10.1016\/j.tjog.2010.07.001","article-title":"Prenatal diagnosis and array comparative genomic hybridization characterization of a de novo interstitial deletion of chromosome 20p","volume":"50","author":"Chen","year":"2011","journal-title":"Taiwan J Obstet Gynecol"},{"key":"10.1016\/j.tjog.2017.04.024_bib6","first-page":"143","article-title":"Allagille's syndrome associated with antenatal ascites","volume":"49","author":"Blanc","year":"1992","journal-title":"Arch Fr Pediatr"},{"key":"10.1016\/j.tjog.2017.04.024_bib7","doi-asserted-by":"crossref","first-page":"232","DOI":"10.1136\/adc.74.3.232","article-title":"Alagille's syndrome associated with cystic renal disease","volume":"74","author":"Martin","year":"1996","journal-title":"Arch Dis Child"},{"key":"10.1016\/j.tjog.2017.04.024_bib8","doi-asserted-by":"crossref","first-page":"582","DOI":"10.1053\/jlts.2000.9739","article-title":"Does liver transplantation affect growth pattern in Alagille syndrome?","volume":"6","author":"Quiros-Tejeira","year":"2000","journal-title":"Liver Transpl"},{"key":"10.1016\/j.tjog.2017.04.024_bib9","doi-asserted-by":"crossref","first-page":"182","DOI":"10.1159\/000048035","article-title":"Alagille syndrome: prenatal diagnosis and pregnancy outcome","volume":"17","author":"Albayram","year":"2002","journal-title":"Fetal Diagn Ther"},{"key":"10.1016\/j.tjog.2017.04.024_bib10","doi-asserted-by":"crossref","first-page":"156","DOI":"10.1002\/jcu.20292","article-title":"Alagille syndrome: prenatal sonographic findings","volume":"35","author":"Ghidini","year":"2007","journal-title":"J\u00a0Clin Ultrasound"},{"key":"10.1016\/j.tjog.2017.04.024_bib11","doi-asserted-by":"crossref","first-page":"450","DOI":"10.3109\/01443615.2011.574749","article-title":"Alagille syndrome","volume":"31","author":"Antsaklis","year":"2011","journal-title":"J\u00a0Obstet Gynaecol"},{"key":"10.1016\/j.tjog.2017.04.024_bib12","doi-asserted-by":"crossref","first-page":"293","DOI":"10.1002\/jcu.22125","article-title":"Two- and three-dimensional prenatal sonographic diagnosis of Alagille syndrome","volume":"42","author":"Wax","year":"2014","journal-title":"J\u00a0Clin Ultrasound"},{"key":"10.1016\/j.tjog.2017.04.024_bib13","doi-asserted-by":"crossref","first-page":"471","DOI":"10.1002\/ajmg.a.37429","article-title":"Discordant clinical phenotype in monozygotic twins with Alagille syndrome: possible influence of non-genetic factors","volume":"170A","author":"Izumi","year":"2016","journal-title":"Am J Med Genet"},{"issue":"4","key":"10.1016\/j.tjog.2017.04.024_bib14","doi-asserted-by":"crossref","first-page":"453","DOI":"10.1097\/MPG.0b013e318036a569","article-title":"Prenatal molecular diagnosis of inherited cholestatic diseases","volume":"44","author":"Jung","year":"2007","journal-title":"J\u00a0Pediatr Gastroenterol Nutr"},{"key":"10.1016\/j.tjog.2017.04.024_bib15","doi-asserted-by":"crossref","first-page":"317","DOI":"10.1002\/pd.1668","article-title":"Advantages of multiple markers and polar body analysis in preimplantation genetic diagnosis for Alagille disease","volume":"27","author":"Renbaum","year":"2007","journal-title":"Prenat Diagn"}],"container-title":["Taiwanese Journal of Obstetrics and Gynecology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1028455917300943?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1028455917300943?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,10,19]],"date-time":"2025-10-19T18:15:21Z","timestamp":1760897721000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S1028455917300943"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2017,6]]},"references-count":15,"journal-issue":{"issue":"3","published-print":{"date-parts":[[2017,6]]}},"alternative-id":["S1028455917300943"],"URL":"https:\/\/doi.org\/10.1016\/j.tjog.2017.04.024","relation":{},"ISSN":["1028-4559"],"issn-type":[{"type":"print","value":"1028-4559"}],"subject":[],"published":{"date-parts":[[2017,6]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Molecular genetic characterization of a prenatally detected de novo interstitial deletion of chromosome 20p (20p12-p13) encompassing JAG1 and a literature review of prenatal diagnosis of Alagille syndrome","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.2017.04.024","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2017 Taiwan Association of Obstetrics & Gynecology. Publishing services by Elsevier B.V.","name":"copyright","label":"Copyright"}]}}