Is an analysis of copy number variants necessary for various types of kidney ultrasound anomalies in fetuses?

BACKGROUND: This study aimed to estimate the associations of copy number variants (CNVs) with fetal kidney ultrasound anomalies. A total of 331 fetuses with kidney ultrasound anomalies who underwent prenatal chromosomal microarray analyses were enrolled. The fetuses were classified into groups with...

Descripción completa

Detalles Bibliográficos
Autores principales: Lin, Shaobin, Shi, Shanshan, Huang, Linhuan, Lei, Ting, Cai, Danlei, Hu, Wenlong, Zhou, Yi, Luo, Yanmin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6610977/
https://www.ncbi.nlm.nih.gov/pubmed/31312255
http://dx.doi.org/10.1186/s13039-019-0443-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6610977/
https://www.ncbi.nlm.nih.gov/pubmed/31312255
http://dx.doi.org/10.1186/s13039-019-0443-3

Ejemplares similares