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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...
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| Vydáno v: | Mol Cytogenet |
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| Hlavní autoři: | , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BioMed Central
2019
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6610977/ https://ncbi.nlm.nih.gov/pubmed/31312255 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13039-019-0443-3 |
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