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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Detalles Bibliográficos
Autores principales: Qi, Yiming, Yang, Jiexia, Hou, Yaping, Hu, Rong, Wang, Dongmei, Peng, Haishan, Yin, Aihua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7249382/
https://www.ncbi.nlm.nih.gov/pubmed/32508984
http://dx.doi.org/10.1186/s13039-020-00485-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7249382/
https://www.ncbi.nlm.nih.gov/pubmed/32508984
http://dx.doi.org/10.1186/s13039-020-00485-3

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