Copy number variants in fetuses with isolated and non-isolated increased nuchal translucency detected by chromosomal microarray analysis.

Saved in:
Bibliographic Details
Title: Copy number variants in fetuses with isolated and non-isolated increased nuchal translucency detected by chromosomal microarray analysis.
Authors: Huang S; Department of Ultrasound, Meizhou People's Hospital, Meizhou Academy of Medical Sciences, Meizhou, China.; Department of Prenatal Diagnostic Center, Meizhou People's Hospital, Meizhou Academy of Medical Sciences, Meizhou, China.; Meizhou Municipal Engineering and Technology Research Center for Molecular Diagnostics of Major Genetic Disorders, Meizhou People's Hospital, Meizhou Academy of Medical Sciences, Meizhou, China., Wu H; Department of Prenatal Diagnostic Center, Meizhou People's Hospital, Meizhou Academy of Medical Sciences, Meizhou, China.; Meizhou Municipal Engineering and Technology Research Center for Molecular Diagnostics of Major Genetic Disorders, Meizhou People's Hospital, Meizhou Academy of Medical Sciences, Meizhou, China., She L; Department of Ultrasound, Meizhou People's Hospital, Meizhou Academy of Medical Sciences, Meizhou, China.; Department of Prenatal Diagnostic Center, Meizhou People's Hospital, Meizhou Academy of Medical Sciences, Meizhou, China.; Meizhou Municipal Engineering and Technology Research Center for Molecular Diagnostics of Major Genetic Disorders, Meizhou People's Hospital, Meizhou Academy of Medical Sciences, Meizhou, China., Liu L; Department of Ultrasound, Meizhou People's Hospital, Meizhou Academy of Medical Sciences, Meizhou, China.; Department of Prenatal Diagnostic Center, Meizhou People's Hospital, Meizhou Academy of Medical Sciences, Meizhou, China.; Meizhou Municipal Engineering and Technology Research Center for Molecular Diagnostics of Major Genetic Disorders, Meizhou People's Hospital, Meizhou Academy of Medical Sciences, Meizhou, China.
Source: Frontiers in genetics [Front Genet] 2025 Dec 18; Vol. 16, pp. 1712025. Date of Electronic Publication: 2025 Dec 18 (Print Publication: 2025).
Publication Type: 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
Full text is not displayed to guests.
Description
ISSN:1664-8021
DOI:10.3389/fgene.2025.1712025