{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,20]],"date-time":"2025-10-20T00:48:28Z","timestamp":1760921308198,"version":"build-2065373602"},"reference-count":14,"publisher":"Elsevier BV","issue":"5","license":[{"start":{"date-parts":[[2023,9,1]],"date-time":"2023-09-01T00:00:00Z","timestamp":1693526400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2023,9,1]],"date-time":"2023-09-01T00:00:00Z","timestamp":1693526400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2023,7,10]],"date-time":"2023-07-10T00:00:00Z","timestamp":1688947200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"funder":[{"DOI":"10.13039\/100020595","name":"National Science and Technology Council","doi-asserted-by":"publisher","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":[[2023,9]]},"DOI":"10.1016\/j.tjog.2023.07.021","type":"journal-article","created":{"date-parts":[[2023,9,7]],"date-time":"2023-09-07T22:18:51Z","timestamp":1694125131000},"page":"754-756","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":0,"title":["Genetic counseling of a prenatally detected familial 18.79-kb Xp21.1 microduplication encompassing exon 13 of DMD in a pregnancy with no apparent phenotypic abnormalities in the male carriers in the family"],"prefix":"10.1016","volume":"62","author":[{"given":"Chih-Ping","family":"Chen","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Shuan-Pei","family":"Lin","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":"Peih-Shan","family":"Wu","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.2023.07.021_bib1","doi-asserted-by":"crossref","first-page":"20","DOI":"10.1186\/1744-9081-4-20","article-title":"Similarity of DMD gene deletion and duplication in the Chinese patients compared to global populations","volume":"4","author":"Wang","year":"2008","journal-title":"Behav Brain Funct"},{"key":"10.1016\/j.tjog.2023.07.021_bib2","doi-asserted-by":"crossref","first-page":"509","DOI":"10.1016\/0092-8674(87)90504-6","article-title":"Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals","volume":"50","author":"Koenig","year":"1987","journal-title":"Cell"},{"key":"10.1016\/j.tjog.2023.07.021_bib3","doi-asserted-by":"crossref","first-page":"109","DOI":"10.1016\/0888-7543(88)90091-2","article-title":"Further studies of gene deletions that cause Duchenne and Becker muscular dystrophies","volume":"2","author":"Forrest","year":"1988","journal-title":"Genomics"},{"key":"10.1016\/j.tjog.2023.07.021_bib4","first-page":"835","article-title":"Topography of the Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplications","volume":"45","author":"Den Dunnen","year":"1989","journal-title":"Am J Hum Genet"},{"key":"10.1016\/j.tjog.2023.07.021_bib5","first-page":"682","article-title":"Duplicational mutation at the Duchenne muscular dystrophy locus: its frequency, distribution, origin, and phenotype-genotype correlation","volume":"46","author":"Hu","year":"1990","journal-title":"Am J Hum Genet"},{"key":"10.1016\/j.tjog.2023.07.021_bib6","doi-asserted-by":"crossref","first-page":"2331","DOI":"10.1073\/pnas.89.6.2331","article-title":"Point mutations in the dystrophin gene","volume":"89","author":"Roberts","year":"1992","journal-title":"Proc Natl Acad Sci USA"},{"key":"10.1016\/j.tjog.2023.07.021_bib7","first-page":"161","article-title":"Clinical value of MLPA in the prenatal gene diagnosis of Duchenne muscular dystrophy","volume":"48","author":"Li","year":"2013","journal-title":"Zhonghua Fu Chan Ke Za Zhi"},{"key":"10.1016\/j.tjog.2023.07.021_bib8","first-page":"773","article-title":"Incidental discovery of DMD gene deletions by chromosomal microarray analysis","volume":"36","author":"Song","year":"2019","journal-title":"Zhonghua Yi Xue Yi Chuan Xue Za Zhi"},{"key":"10.1016\/j.tjog.2023.07.021_bib9","first-page":"226","article-title":"Genetic analysis and prenatal diagnosis of Duchenne or Becker muscular dystrophy","volume":"54","author":"Zhao","year":"2019","journal-title":"Zhonghua Fu Chan Ke Za Zhi"},{"key":"10.1016\/j.tjog.2023.07.021_bib10","first-page":"669","article-title":"Analysis of results of prenatal diagnosis for 67 pedigrees affected with Duchenne muscular dystrophy in the central plain region of China","volume":"39","author":"Gao","year":"2022","journal-title":"Zhonghua Yi Xue Yi Chuan Xue Za Zhi"},{"issue":"5","key":"10.1016\/j.tjog.2023.07.021_bib11","article-title":"Chromosome microarray analysis detection of a single exon deletion of the Duchenne muscular dystrophy gene in a fetus: a case report","volume":"68","author":"Wang","year":"2022","journal-title":"Clin Lab"},{"key":"10.1016\/j.tjog.2023.07.021_bib12","doi-asserted-by":"crossref","first-page":"1972","DOI":"10.3390\/genes13111972","article-title":"Reclassification of DMD duplications as benign: recommendations for cautious interpretation of variants identified in prenatal screening","volume":"13","author":"He","year":"2022","journal-title":"Genes (Basel)"},{"key":"10.1016\/j.tjog.2023.07.021_bib13","doi-asserted-by":"crossref","first-page":"139","DOI":"10.1186\/s12881-019-0873-0","article-title":"Genetic analysis of 1051 Chinese families with Duchenne\/Becker muscular dystrophy","volume":"20","author":"Kong","year":"2019","journal-title":"BMC Med Genet"},{"key":"10.1016\/j.tjog.2023.07.021_bib14","first-page":"547","article-title":"A\u00a015-year molecular analysis of DMD\/BMD: genetic features in a large cohort","volume":"2","author":"Carsana","year":"2010","journal-title":"Front Biosci (Elite Ed)"}],"container-title":["Taiwanese Journal of Obstetrics and Gynecology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1028455923001948?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1028455923001948?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,10,19]],"date-time":"2025-10-19T18:21:51Z","timestamp":1760898111000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S1028455923001948"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2023,9]]},"references-count":14,"journal-issue":{"issue":"5","published-print":{"date-parts":[[2023,9]]}},"alternative-id":["S1028455923001948"],"URL":"https:\/\/doi.org\/10.1016\/j.tjog.2023.07.021","relation":{},"ISSN":["1028-4559"],"issn-type":[{"type":"print","value":"1028-4559"}],"subject":[],"published":{"date-parts":[[2023,9]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Genetic counseling of a prenatally detected familial 18.79-kb Xp21.1 microduplication encompassing exon 13 of DMD in a pregnancy with no apparent phenotypic abnormalities in the male carriers in the family","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.2023.07.021","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"}]}}