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Prenatal whole‐exome sequencing in fetuses with increased nuchal translucency
BACKGROUND: Increased nuchal translucency (NT) is associated with an increased risk for genetic disorders. The aim of this study was to investigate the value of whole‐exome sequencing (WES) in detecting genetic abnormalities for fetuses with isolated first‐trimester increased NT. METHODS: After the...
Autores principales: | Cao, Chunge, Liu, Fang, Yang, Yan, Zhang, Qing, Huang, Junfang, Liu, Xinhong |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10655512/ https://www.ncbi.nlm.nih.gov/pubmed/37766479 http://dx.doi.org/10.1002/mgg3.2246 |
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