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Potential influence of parental copy number variations on noninvasive prenatal testing (NIPT): two case reports
BACKGROUND: Small subchromosomal deletions and duplications caused by copy number variants (CNVs) can now be detected with noninvasive prenatal testing (NIPT) technology. However, the clinical utility and validity of this screening for CNVs are still unknown. Here, we discuss some special conditions...
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| Publicado en: | Mol Cytogenet |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
BioMed Central
2020
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7249382/ https://ncbi.nlm.nih.gov/pubmed/32508984 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13039-020-00485-3 |
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