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Case Report: Expanding the diagnostic spectrum of non-invasive prenatal testing to structural chromosomal abnormalities.

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Title: Case Report: Expanding the diagnostic spectrum of non-invasive prenatal testing to structural chromosomal abnormalities.
Authors: Kim JC; Center for Genome Diagnostics, CHA Biotech Inc., Seoul, Republic of Korea., Kim H; Center for Genome Diagnostics, CHA Biotech Inc., Seoul, Republic of Korea., Jang H; Center for Genome Diagnostics, CHA Biotech Inc., Seoul, Republic of Korea.; Department of Biomedical Science, College of Life Science, CHA University, Seongnam-si, Republic of Korea., Go M; Center for Genome Diagnostics, CHA Biotech Inc., Seoul, Republic of Korea.; Department of Biomedical Science, College of Life Science, CHA University, Seongnam-si, Republic of Korea., Park JE; Center for Genome Diagnostics, CHA Biotech Inc., Seoul, Republic of Korea., Ryu CS; Department of Biomedical Science, College of Life Science, CHA University, Seongnam-si, Republic of Korea., Chin MU; Center for Genome Diagnostics, CHA Biotech Inc., Seoul, Republic of Korea., Kim EH; Center for Genome Diagnostics, CHA Biotech Inc., Seoul, Republic of Korea., Lee YJ; Center for Genome Diagnostics, CHA Biotech Inc., Seoul, Republic of Korea., Shim SH; Department of Biomedical Science, College of Life Science, CHA University, Seongnam-si, Republic of Korea., Cha DH; Department of Obstetrics and Gynecology, CHA Gangnam Medical Center, CHA University, Seoul, Republic of Korea.
Source: Frontiers in genetics [Front Genet] 2026 Feb 17; Vol. 17, pp. 1746287. Date of Electronic Publication: 2026 Feb 17 (Print Publication: 2026).
Publication Type: Case Reports; Journal Article
Journal Info: Publisher: Frontiers Research Foundation Country of Publication: Switzerland NLM ID: 101560621 Publication Model: eCollection Cited Medium: Print ISSN: 1664-8021 (Print) Linking ISSN: 16648021 NLM ISO Abbreviation: Front Genet Subsets: PubMed not MEDLINE
Database: MEDLINE Ultimate
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  Data: Case Report: Expanding the diagnostic spectrum of non-invasive prenatal testing to structural chromosomal abnormalities.
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  Data: <searchLink fieldCode="AU" term="%22Kim+JC%22">Kim JC</searchLink>; Center for Genome Diagnostics, CHA Biotech Inc., Seoul, Republic of Korea.<br /><searchLink fieldCode="AU" term="%22Kim+H%22">Kim H</searchLink>; Center for Genome Diagnostics, CHA Biotech Inc., Seoul, Republic of Korea.<br /><searchLink fieldCode="AU" term="%22Jang+H%22">Jang H</searchLink>; Center for Genome Diagnostics, CHA Biotech Inc., Seoul, Republic of Korea.; Department of Biomedical Science, College of Life Science, CHA University, Seongnam-si, Republic of Korea.<br /><searchLink fieldCode="AU" term="%22Go+M%22">Go M</searchLink>; Center for Genome Diagnostics, CHA Biotech Inc., Seoul, Republic of Korea.; Department of Biomedical Science, College of Life Science, CHA University, Seongnam-si, Republic of Korea.<br /><searchLink fieldCode="AU" term="%22Park+JE%22">Park JE</searchLink>; Center for Genome Diagnostics, CHA Biotech Inc., Seoul, Republic of Korea.<br /><searchLink fieldCode="AU" term="%22Ryu+CS%22">Ryu CS</searchLink>; Department of Biomedical Science, College of Life Science, CHA University, Seongnam-si, Republic of Korea.<br /><searchLink fieldCode="AU" term="%22Chin+MU%22">Chin MU</searchLink>; Center for Genome Diagnostics, CHA Biotech Inc., Seoul, Republic of Korea.<br /><searchLink fieldCode="AU" term="%22Kim+EH%22">Kim EH</searchLink>; Center for Genome Diagnostics, CHA Biotech Inc., Seoul, Republic of Korea.<br /><searchLink fieldCode="AU" term="%22Lee+YJ%22">Lee YJ</searchLink>; Center for Genome Diagnostics, CHA Biotech Inc., Seoul, Republic of Korea.<br /><searchLink fieldCode="AU" term="%22Shim+SH%22">Shim SH</searchLink>; Department of Biomedical Science, College of Life Science, CHA University, Seongnam-si, Republic of Korea.<br /><searchLink fieldCode="AU" term="%22Cha+DH%22">Cha DH</searchLink>; Department of Obstetrics and Gynecology, CHA Gangnam Medical Center, CHA University, Seoul, Republic of Korea.
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  Data: <searchLink fieldCode="JN" term="%22101560621%22">Frontiers in genetics</searchLink> [Front Genet] 2026 Feb 17; Vol. 17, pp. 1746287. <i>Date of Electronic Publication: </i>2026 Feb 17 (<i>Print Publication: </i>2026).
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Frontiers+Research+Foundation%22">Frontiers Research Foundation </searchLink><i>Country of Publication: </i>Switzerland <i>NLM ID: </i>101560621 <i>Publication Model: </i>eCollection <i>Cited Medium: </i>Print <i>ISSN: </i>1664-8021 (Print) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2216648021%22">16648021 </searchLink><i>NLM ISO Abbreviation: </i>Front Genet <i>Subsets: </i>PubMed not MEDLINE
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=41778171
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              Text: 2026 Feb 17
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