Detection of copy number variation associated with ventriculomegaly in fetuses using single nucleotide polymorphism arrays

Etiopathogenesis of fetal ventriculomegaly is poorly understood. Associations between fetal isolated ventriculomegaly and copy number variations (CNVs) have been previously described. We investigated the correlations between fetal ventriculomegaly—with or without other ultrasound anomalies—and chrom...

Descripción completa

Detalles Bibliográficos
Autores principales: Xue, Huili, Yu, Aili, Lin, Na, Chen, Xuemei, Lin, Min, Wang, Yan, Huang, Hailong, Xu, Liangpu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7935846/
https://www.ncbi.nlm.nih.gov/pubmed/33674646
http://dx.doi.org/10.1038/s41598-021-83147-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7935846/
https://www.ncbi.nlm.nih.gov/pubmed/33674646
http://dx.doi.org/10.1038/s41598-021-83147-7

Ejemplares similares