{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,3,7]],"date-time":"2026-03-07T00:02:46Z","timestamp":1772841766854,"version":"3.50.1"},"reference-count":12,"publisher":"Wiley","issue":"4","license":[{"start":{"date-parts":[[2019,2,20]],"date-time":"2019-02-20T00:00:00Z","timestamp":1550620800000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":["obgyn.onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Prenatal Diagnosis"],"published-print":{"date-parts":[[2019,3]]},"abstract":"<jats:p>What's already known about this topic?\n<jats:list list-type=\"bullet\">\n<jats:list-item><jats:p>The false positive rate of detecting monosomy X by NIPT is higher than that of other autosomal aneuploidies, due in part to maternal mosaic monosomy X.<\/jats:p><\/jats:list-item>\n<\/jats:list><\/jats:p><jats:p>What does this study add?\n<jats:list list-type=\"bullet\">\n<jats:list-item><jats:p>Our triSure method is less sensitive to the confounding effect of maternal DNA than NIPTeR method.<\/jats:p><\/jats:list-item>\n<jats:list-item><jats:p>By combining <jats:italic>z<\/jats:italic>\u2010scores of chrX from triSure and NIPTeR, we can detect cases of fetal XX (\u22122.5\u00a0&lt;\u00a0z<jats:sub>X by triSure<\/jats:sub>\u00a0&lt;\u00a02.5) with maternal mosaicism monosomy X (z<jats:sub>X by NIPTeR<\/jats:sub>\u00a0&lt;\u00a0\u22122.5), potentially reducing false positive rate of fetal monosomy X.<\/jats:p><\/jats:list-item>\n<\/jats:list><\/jats:p>","DOI":"10.1002\/pd.5430","type":"journal-article","created":{"date-parts":[[2019,2,5]],"date-time":"2019-02-05T10:34:17Z","timestamp":1549362857000},"page":"324-327","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":6,"title":["Reducing false positive rate of fetal monosomy X in non\u2010invasive prenatal testing using a combined algorithm to detect maternal mosaic monosomy X"],"prefix":"10.1002","volume":"39","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-3426-1044","authenticated-orcid":false,"given":"Minh\u2010Duy","family":"Phan","sequence":"first","affiliation":[{"name":"Gene Solutions  Ho Chi Minh City Vietnam"},{"name":"School of Chemistry and Molecular Biosciences The University of Queensland  Brisbane Australia"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Binh T.","family":"Vo","sequence":"additional","affiliation":[{"name":"Center for Molecular Medicine University of Medicine and Pharmacy  Ho Chi Minh City Vietnam"},{"name":"Graduate Program of Genetics Ho Chi Minh City University of Science  Ho Chi Minh City Vietnam"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Thong V.","family":"Nguyen","sequence":"additional","affiliation":[{"name":"Hung Vuong Hospital  Ho Chi Minh City 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