SNP-Based Chromosomal Microarray Analysis for Detecting DNA Copy Number Variations in Fetuses with a Thickened Nuchal Fold

The aim of the study was to assess the diagnostic potential of SNP-based chromosomal microarray analysis for detecting pathogenic copies number variations (CNVs) in fetuses with a normal karyotype, in which an increase in the nuchal translucence of >2.5 mm was detected by ultrasound at a gestatio...

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Detalles Bibliográficos
Autores principales: Kievskaya, J.K., Shilova, N.V., Kanivets, I.V., Kudryavtseva, E.V., Pyankov, D.V., Korostelev, S.A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Privolzhsky Research Medical University 2021
Materias:
Clinical Supplements
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8858397/
https://www.ncbi.nlm.nih.gov/pubmed/35265361
http://dx.doi.org/10.17691/stm2021.13.6.08

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8858397/
https://www.ncbi.nlm.nih.gov/pubmed/35265361
http://dx.doi.org/10.17691/stm2021.13.6.08

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