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Detection of copy number variation associated with ventriculomegaly in fetuses using single nucleotide polymorphism arrays
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—and chrom...
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| Publicado no: | Sci Rep |
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| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Nature Publishing Group UK
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7935846/ https://ncbi.nlm.nih.gov/pubmed/33674646 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-021-83147-7 |
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