{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,6,2]],"date-time":"2026-06-02T14:59:45Z","timestamp":1780412385759,"version":"3.54.1"},"reference-count":12,"publisher":"Elsevier BV","issue":"3","license":[{"start":{"date-parts":[[2019,5,1]],"date-time":"2019-05-01T00:00:00Z","timestamp":1556668800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2019,5,1]],"date-time":"2019-05-01T00:00:00Z","timestamp":1556668800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2019,3,8]],"date-time":"2019-03-08T00:00:00Z","timestamp":1552003200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"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":[[2019,5]]},"DOI":"10.1016\/j.tjog.2019.03.005","type":"journal-article","created":{"date-parts":[[2019,5,20]],"date-time":"2019-05-20T07:39:34Z","timestamp":1558337974000},"page":"318-323","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":5,"title":["Prenatal diagnosis and molecular cytogenetic characterization of partial dup(18q)\/del(18p) due to a paternal pericentric inversion 18 in a fetus with multiple anomalies"],"prefix":"10.1016","volume":"58","author":[{"given":"Min Jin","family":"Lee","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sang Hee","family":"Park","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sung Han","family":"Shim","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Myoung-jin","family":"Moon","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Dong Hyun","family":"Cha","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1016\/j.tjog.2019.03.005_bib1","doi-asserted-by":"crossref","first-page":"143","DOI":"10.1002\/ajmg.a.37976","article-title":"A\u00a0boy with partial dup (18q)\/del (18p) due to a maternal pericentric inversion: genotype\u2013phenotype correlation and risk of recombinant chromosomes based on systematic review of the literature","volume":"173","author":"Lustosa-Mendes","year":"2017","journal-title":"Am J Med Genet"},{"key":"10.1016\/j.tjog.2019.03.005_bib2","doi-asserted-by":"crossref","first-page":"520","DOI":"10.1111\/j.1399-0004.1996.tb02726.x","article-title":"Partial deletion of 18p and partial duplication of 18q caused by a paternal pericentric inversion","volume":"50","author":"Isra\u00ebls","year":"1996","journal-title":"Clin Genet"},{"key":"10.1016\/j.tjog.2019.03.005_bib3","doi-asserted-by":"crossref","first-page":"297","DOI":"10.1159\/000086903","article-title":"Sperm studies in heterozygote inversion carriers: a review","volume":"111","author":"Anton","year":"2005","journal-title":"Cytogenet Genome Res"},{"key":"10.1016\/j.tjog.2019.03.005_bib4","doi-asserted-by":"crossref","first-page":"947","DOI":"10.1002\/1097-0223(200012)20:12<947::AID-PD957>3.0.CO;2-X","article-title":"Prenatal diagnosis of holoprosencephaly (HPE) in a fetus with a recombinant (18) dup (18q) inv (18)(p11. 31q11. 2) mat","volume":"20","author":"Leonard","year":"2000","journal-title":"Prenat Diagn"},{"key":"10.1016\/j.tjog.2019.03.005_bib5","doi-asserted-by":"crossref","first-page":"65","DOI":"10.1159\/000053884","article-title":"Congenital Cystic adenomatoid malformation of the lung coexisting with recombinant chromosome 18","volume":"16","author":"Roberts","year":"2001","journal-title":"Fetal Diagn Ther"},{"key":"10.1016\/j.tjog.2019.03.005_bib6","doi-asserted-by":"crossref","first-page":"182","DOI":"10.1016\/j.tjog.2011.04.001","article-title":"Prenatal diagnosis and molecular cytogenetic characterization of a derivative chromosome der (18; 18)(q10; q10) del (18)(q11. 1q12. 1) del (18)(q22. 1q22. 3) presenting as apparent isochromosome 18q in a fetus with holoprosencephaly","volume":"50","author":"Chen","year":"2011","journal-title":"Taiwan J Obstet Gynecol"},{"key":"10.1016\/j.tjog.2019.03.005_bib7","doi-asserted-by":"crossref","first-page":"258","DOI":"10.1055\/s-0037-1604099","article-title":"A\u00a0Peruvian child with 18p-\/18q+ syndrome and persistent microscopic hematuria","volume":"6","author":"Poterico","year":"2017","journal-title":"J\u00a0Pediatr Genet"},{"key":"10.1016\/j.tjog.2019.03.005_bib8","doi-asserted-by":"crossref","first-page":"733","DOI":"10.1016\/j.tjog.2016.07.007","article-title":"Prenatal diagnosis and molecular cytogenetic characterization of rec (10) dup (10p) inv (10)(p11. 2q26. 3) in a fetus associated with paternal pericentric inversion","volume":"55","author":"Chen","year":"2016","journal-title":"Taiwan J Obstet Gynecol"},{"key":"10.1016\/j.tjog.2019.03.005_bib9","doi-asserted-by":"crossref","first-page":"251","DOI":"10.1002\/ajmg.c.31445","article-title":"A\u00a0review of 18p deletions","volume":"169","author":"Hasi-Zogaj","year":"2015","journal-title":"Am J Med Genet C \u2013 Semin Med Genet"},{"key":"10.1016\/j.tjog.2019.03.005_bib10","doi-asserted-by":"crossref","first-page":"628","DOI":"10.1002\/ca.22725","article-title":"Anatomy of trisomy 18","volume":"29","author":"Roberts","year":"2016","journal-title":"Clin Anat"},{"key":"10.1016\/j.tjog.2019.03.005_bib11","first-page":"476","article-title":"Molecular mapping of the Edwards syndrome phenotype to two\u00a0noncontiguous regions on chromosome 18","volume":"55","author":"Boghosian-Sell","year":"1994","journal-title":"Am J Hum Genet"},{"key":"10.1016\/j.tjog.2019.03.005_bib12","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1007\/BF00293765","article-title":"Risk for recombinants in pericentric inversions of the (p11\u2192 q21) region of chromosome 18","volume":"37","author":"Vigi","year":"1977","journal-title":"Hum Genet"}],"container-title":["Taiwanese Journal of Obstetrics and Gynecology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1028455919300622?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1028455919300622?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,10,19]],"date-time":"2025-10-19T18:16:22Z","timestamp":1760897782000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S1028455919300622"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2019,5]]},"references-count":12,"journal-issue":{"issue":"3","published-print":{"date-parts":[[2019,5]]}},"alternative-id":["S1028455919300622"],"URL":"https:\/\/doi.org\/10.1016\/j.tjog.2019.03.005","relation":{},"ISSN":["1028-4559"],"issn-type":[{"value":"1028-4559","type":"print"}],"subject":[],"published":{"date-parts":[[2019,5]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Prenatal diagnosis and molecular cytogenetic characterization of partial dup(18q)\/del(18p) due to a paternal pericentric inversion 18 in a fetus with multiple anomalies","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.2019.03.005","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"}]}}