{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,11,30]],"date-time":"2025-11-30T09:10:03Z","timestamp":1764493803096},"reference-count":10,"publisher":"Wiley","issue":"3","license":[{"start":{"date-parts":[[2013,12,23]],"date-time":"2013-12-23T00:00:00Z","timestamp":1387756800000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Prenatal Diagnosis"],"published-print":{"date-parts":[[2014,3]]},"abstract":"<jats:p><jats:bold>What<\/jats:bold>'<jats:bold>s already known about this topic<\/jats:bold>?  \n<jats:list list-type=\"bullet\">\n<jats:list-item><jats:p>Mowat\u2013Wilson syndrome (MWS) (OMIM#235730) is a genetic disease caused by mutations or deletions of the <jats:italic>ZEB2<\/jats:italic> gene and characterized by typical facial dysmorphism. It is rarely diagnosed prenatally.<\/jats:p><\/jats:list-item><\/jats:list><\/jats:p><jats:p><jats:bold>What does this study add<\/jats:bold>?  \n<jats:list list-type=\"bullet\">\n<jats:list-item><jats:p>We report and review the ultrasound features of MWS fetuses identified by array comparative genomic hybridization study.<\/jats:p><\/jats:list-item>\n<jats:list-item><jats:p>The MWS should be considered in fetuses with increased nuchal translucency, ACC, hypospadias, and congenital heart defect.<\/jats:p><\/jats:list-item>\n<jats:list-item><jats:p>The prevalence of MWS in Hong Kong is reported.<\/jats:p><\/jats:list-item><\/jats:list><\/jats:p>","DOI":"10.1002\/pd.4292","type":"journal-article","created":{"date-parts":[[2013,12,4]],"date-time":"2013-12-04T03:48:53Z","timestamp":1386128933000},"page":"296-298","source":"Crossref","is-referenced-by-count":6,"title":["Recurrent structural malformations identified among Mowat\u2013Wilson syndrome fetuses"],"prefix":"10.1002","volume":"34","author":[{"given":"Yan","family":"Zhou","sequence":"first","affiliation":[{"name":"Department of Obstetrics and Gynaecology Wuhan Medical Care Center for Women and Children  Wuhan China"},{"name":"Fetal Medicine Unit, Department of Obstetrics and Gynaecology The Chinese University of Hong Kong, Prince of Wales Hospital  Hong Kong China"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jin","family":"Huang","sequence":"additional","affiliation":[{"name":"Fetal Medicine Unit, Department of Obstetrics and Gynaecology The Chinese University of Hong Kong, Prince of Wales Hospital  Hong Kong China"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Yvonne Kwun Yue","family":"Cheng","sequence":"additional","affiliation":[{"name":"Fetal Medicine Unit, Department of Obstetrics and Gynaecology The Chinese University of Hong Kong, Prince of Wales Hospital  Hong Kong China"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Tak Yeung","family":"Leung","sequence":"additional","affiliation":[{"name":"Fetal Medicine Unit, Department of Obstetrics and Gynaecology The Chinese University of Hong Kong, Prince of Wales Hospital  Hong Kong China"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ritsuko K.","family":"Pooh","sequence":"additional","affiliation":[{"name":"CRIFM Clinical Research Institute of Fetal Medicine PMC  Osaka Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Fai Man","family":"Lo","sequence":"additional","affiliation":[{"name":"Clinical Genetics Service Department of Health  Hong Kong China"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Kwong Wai","family":"Choy","sequence":"additional","affiliation":[{"name":"Fetal Medicine Unit, Department of Obstetrics and Gynaecology The Chinese University of Hong Kong, Prince of Wales Hospital  Hong Kong China"},{"name":"Joint Centre with Utrecht University\u2010Genetic Core The Chinese University of Hong Kong  Hong Kong China"},{"name":"Shenzhen Research Institute, The Chinese University of Hong Kong  Hong Kong Hong 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