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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...
Autores principales: | Lin, Shaobin, Shi, Shanshan, Huang, Linhuan, Lei, Ting, Cai, Danlei, Hu, Wenlong, Zhou, Yi, Luo, Yanmin |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
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 |
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