A clear bias in parental origin of de novo pathogenic CNVs related to intellectual disability, developmental delay and multiple congenital anomalies

Copy number variation (CNV) is of great significance in human evolution and disorders. Through tracing the parent-of-origin of de novo pathogenic CNVs, we are expected to investigate the relative contributions of germline genomic stability on reproductive health. In our study, short tandem repeat (S...

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Detalles Bibliográficos
Autores principales: Ma, Ruiyu, Deng, Linbei, Xia, Yan, Wei, Xianda, Cao, Yingxi, Guo, Ruolan, Zhang, Rui, Guo, Jing, Liang, Desheng, Wu, Lingqian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5359547/
https://www.ncbi.nlm.nih.gov/pubmed/28322228
http://dx.doi.org/10.1038/srep44446

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5359547/
https://www.ncbi.nlm.nih.gov/pubmed/28322228
http://dx.doi.org/10.1038/srep44446

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