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

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

Abstract 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—...

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Autores principales: Huili Xue, Aili Yu, Na Lin, Xuemei Chen, Min Lin, Yan Wang, Hailong Huang, Liangpu Xu
Formato: article
Lenguaje:EN
Publicado: Nature Portfolio 2021
Materias:
Medicine
R
Science
Q
Acceso en línea:https://doaj.org/article/37d796801dc5425589fe3bf0cbd7d314
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