Validity and Utility of Non-Invasive Prenatal Testing for Copy Number Variations and Microdeletions: A Systematic Review

Valid data on prenatal cell-free DNA-based screening tests for copy number variations and microdeletions are still insufficient. We aimed to compare different methodological approaches concerning the achieved diagnostic accuracy measurements and positive predictive values. For this systematic review...

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Detalles Bibliográficos
Autores principales: Zaninović, Luca, Bašković, Marko, Ježek, Davor, Katušić Bojanac, Ana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Systematic Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9224664/
https://www.ncbi.nlm.nih.gov/pubmed/35743413
http://dx.doi.org/10.3390/jcm11123350

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9224664/
https://www.ncbi.nlm.nih.gov/pubmed/35743413
http://dx.doi.org/10.3390/jcm11123350

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