Is an analysis of copy number variants necessary for various types of kidney ultrasound anomalies in fetuses?
Abstract 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 grou...
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| Principais autores: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BMC
2019-07-01
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| coleção: | Molecular Cytogenetics |
| Assuntos: | |
| Acesso em linha: | http://link.springer.com/article/10.1186/s13039-019-0443-3 |
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