Whole-exome sequencing in deceased fetuses with ultrasound anomalies: a retrospective analysis

BACKGROUND: Whole-exome sequencing (WES) is an effective method in the prenatal setting for identification of the underlying genetic etiology of fetal ultrasound abnormalities. To investigate the diagnostic value of WES in fetuses with ultrasound abnormalities that resulted in fetal demise or pregna...

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Detalles Bibliográficos
Autores principales: Huang, Wei, Zhu, Xiaofan, Sun, Gege, Gao, Zhi, Kong, Xiangdong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9936674/
https://www.ncbi.nlm.nih.gov/pubmed/36797717
http://dx.doi.org/10.1186/s12920-022-01427-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9936674/
https://www.ncbi.nlm.nih.gov/pubmed/36797717
http://dx.doi.org/10.1186/s12920-022-01427-1

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