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...

Descripción completa

Detalles Bibliográficos
Autores principales: Cao, Chunge, Liu, Fang, Yang, Yan, Zhang, Qing, Huang, Junfang, Liu, Xinhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Original Articles
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

Internet

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

Ejemplares similares