{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,1,25]],"date-time":"2026-01-25T23:25:13Z","timestamp":1769383513148,"version":"3.49.0"},"reference-count":18,"publisher":"Elsevier BV","issue":"5","license":[{"start":{"date-parts":[[2018,10,1]],"date-time":"2018-10-01T00:00:00Z","timestamp":1538352000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2018,10,1]],"date-time":"2018-10-01T00:00:00Z","timestamp":1538352000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2018,8,15]],"date-time":"2018-08-15T00:00:00Z","timestamp":1534291200000},"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\/501100004663","name":"Ministry of Science and Technology, Taiwan","doi-asserted-by":"publisher","award":["MMH-E-106-04"],"award-info":[{"award-number":["MMH-E-106-04"]}],"id":[{"id":"10.13039\/501100004663","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":[[2018,10]]},"DOI":"10.1016\/j.tjog.2018.08.023","type":"journal-article","created":{"date-parts":[[2018,10,17]],"date-time":"2018-10-17T16:50:54Z","timestamp":1539795054000},"page":"734-738","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":12,"title":["Prenatal diagnosis of a familial 5p14.3-p14.1 deletion encompassing CDH18, CDH12, PMCHL1, PRDM9 and CDH10 in a fetus with congenital heart disease on prenatal ultrasound"],"prefix":"10.1016","volume":"57","author":[{"given":"Chih-Ping","family":"Chen","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Shu-Yuan","family":"Chang","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Chen-Ju","family":"Lin","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":"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":"Tzu-Yun","family":"Chuang","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Wen-Lin","family":"Chen","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Chien-Wen","family":"Yang","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.2018.08.023_bib1","doi-asserted-by":"crossref","first-page":"312","DOI":"10.1086\/427762","article-title":"High-resolution mapping of genotype-phenotype relationships in cri du chat syndrome using array comparative genomic hybridization","volume":"76","author":"Zhang","year":"2005","journal-title":"Am J Hum Genet"},{"key":"10.1016\/j.tjog.2018.08.023_bib2","first-page":"562","article-title":"A\u00a0fine structure physical map of the short arm of chromosome 5","volume":"39","author":"Overhauser","year":"1986","journal-title":"Am J Hum Genet"},{"key":"10.1016\/j.tjog.2018.08.023_bib3","doi-asserted-by":"crossref","first-page":"144","DOI":"10.1002\/(SICI)1097-0223(200002)20:2<144::AID-PD770>3.0.CO;2-9","article-title":"Inherited interstitial deletion of chromosomes 5p and 16q without apparent phenotypic effect: further confirmation","volume":"20","author":"Hand","year":"2000","journal-title":"Prenat Diagn"},{"key":"10.1016\/j.tjog.2018.08.023_bib4","doi-asserted-by":"crossref","first-page":"125","DOI":"10.1136\/jmg.37.2.125","article-title":"5p14 deletion associated with microcephaly and seizures","volume":"37","author":"Johnson","year":"2000","journal-title":"J\u00a0Med Genet"},{"key":"10.1016\/j.tjog.2018.08.023_bib5","unstructured":"DECIPHER database: Database of Chromosomal Imbalance and Phenotype in Humans using Ensembl Resources. Available at: http:\/\/decipher.sanger.ac.uk\/. [Accessed 27 October 2017 ]."},{"key":"10.1016\/j.tjog.2018.08.023_bib6","doi-asserted-by":"crossref","first-page":"130","DOI":"10.1016\/j.brainres.2012.06.020","article-title":"Cadherins and neuropsychiatric disorders","volume":"1470","author":"Redies","year":"2012","journal-title":"Brain Res"},{"key":"10.1016\/j.tjog.2018.08.023_bib7","doi-asserted-by":"crossref","first-page":"528","DOI":"10.1038\/nature07999","article-title":"Common genetic variants on 5p14.1 associate with autism spectrum disorders","volume":"459","author":"Wang","year":"2009","journal-title":"Nature"},{"key":"10.1016\/j.tjog.2018.08.023_bib8","doi-asserted-by":"crossref","first-page":"23","DOI":"10.1192\/bjp.bp.108.061424","article-title":"Genetic utility of broadly defined bipolar schizoaffective disorder as a diagnostic concept","volume":"195","author":"Hamshere","year":"2009","journal-title":"Br J Psychiatry"},{"key":"10.1016\/j.tjog.2018.08.023_bib9","doi-asserted-by":"crossref","DOI":"10.1371\/journal.pone.0153864","article-title":"Genetic candidate variants in two multigenerational families with childhood apraxia of speech","volume":"11","author":"Peter","year":"2016","journal-title":"PLoS One"},{"key":"10.1016\/j.tjog.2018.08.023_bib10","doi-asserted-by":"crossref","first-page":"44155","DOI":"10.1038\/srep44155","article-title":"Genome-wide copy number variation analysis in a Chinese autism spectrum disorder cohort","volume":"7","author":"Guo","year":"2017","journal-title":"Sci Rep"},{"key":"10.1016\/j.tjog.2018.08.023_bib11","first-page":"2473","article-title":"A\u00a0novel relationship for schizophrenia, bipolar and major depressive disorder Part 5: a hint from chromosome 5 high density association screen","volume":"9","author":"Chen","year":"2017","journal-title":"Am J Transl Res"},{"key":"10.1016\/j.tjog.2018.08.023_bib12","doi-asserted-by":"crossref","DOI":"10.1038\/tp.2015.177","article-title":"Brain-specific epigenetic markers of schizophrenia","volume":"5","author":"Wockner","year":"2015","journal-title":"Transl Psychiatry"},{"key":"10.1016\/j.tjog.2018.08.023_bib13","doi-asserted-by":"crossref","first-page":"971","DOI":"10.1042\/BCJ20161067","article-title":"Discovery and characterisation of the automethylation properties of PRDM9","volume":"474","author":"Koh-Stenta","year":"2017","journal-title":"Biochem J"},{"key":"10.1016\/j.tjog.2018.08.023_bib14","doi-asserted-by":"crossref","first-page":"681","DOI":"10.1007\/s00412-017-0631-z","article-title":"The PRDM9 KRAB domain is required for meiosis and involved in protein interactions","volume":"126","author":"Imai","year":"2017","journal-title":"Chromosoma"},{"key":"10.1016\/j.tjog.2018.08.023_bib15","doi-asserted-by":"crossref","first-page":"40031","DOI":"10.1038\/srep40031","article-title":"An exploratory study of predisposing genetic factors for DiGeorge\/velocardiofacial syndrome","volume":"7","author":"Verg\u00e9s","year":"2017","journal-title":"Sci Rep"},{"key":"10.1016\/j.tjog.2018.08.023_bib16","doi-asserted-by":"crossref","first-page":"31","DOI":"10.1006\/geno.1994.1008","article-title":"Assignment of the human pro-melanin-concentrating hormone gene (PMCH) to chromosome 12q23-q24 and two variant genes (PMCHL1 and PMCHL2) to chromosome 5p14 and 5q12-q13","volume":"19","author":"Pedeutour","year":"1994","journal-title":"Genomics"},{"key":"10.1016\/j.tjog.2018.08.023_bib17","doi-asserted-by":"crossref","first-page":"86","DOI":"10.1016\/S0006-8993(98)00626-X","article-title":"Antisense expression of the human pro-melanin-concentrating hormone genes","volume":"803","author":"Miller","year":"1998","journal-title":"Brain Res"},{"key":"10.1016\/j.tjog.2018.08.023_bib18","doi-asserted-by":"crossref","first-page":"1626","DOI":"10.1093\/oxfordjournals.molbev.a026262","article-title":"Structure and expression of the variant melanin-concentrating hormone genes: only PMCHL1 is transcribed in the developing human brain and encodes a putative protein","volume":"17","author":"Viale","year":"2000","journal-title":"Mol Biol Evol"}],"container-title":["Taiwanese Journal of Obstetrics and Gynecology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1028455918301906?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1028455918301906?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,10,19]],"date-time":"2025-10-19T18:16:47Z","timestamp":1760897807000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S1028455918301906"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2018,10]]},"references-count":18,"journal-issue":{"issue":"5","published-print":{"date-parts":[[2018,10]]}},"alternative-id":["S1028455918301906"],"URL":"https:\/\/doi.org\/10.1016\/j.tjog.2018.08.023","relation":{},"ISSN":["1028-4559"],"issn-type":[{"value":"1028-4559","type":"print"}],"subject":[],"published":{"date-parts":[[2018,10]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Prenatal diagnosis of a familial 5p14.3-p14.1 deletion encompassing CDH18, CDH12, PMCHL1, PRDM9 and CDH10 in a fetus with congenital heart disease on prenatal ultrasound","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.2018.08.023","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2018 Taiwan Association of Obstetrics & Gynecology. Publishing services by Elsevier B.V.","name":"copyright","label":"Copyright"}]}}