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. |
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| 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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| ISSN: | 1664-8021 |
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| DOI: | 10.3389/fgene.2026.1746287 |
