Distribution and transmission of copy number variations of uncertain significance in 105 trios

BACKGROUND: The distribution and genetic characteristics of copy number variations (CNVs) remain unclear. Here, we investigated the distribution and transmission of CNVs of uncertain significance in fetuses. METHODS: Low‐coverage massively parallels CNV sequencing of 105 families (parents and their...

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Detalles Bibliográficos
Autores principales: Wen, Qiang, Wang, Xiu, Zhang, Hao, Liu, Xiaoyan, Xu, Zhihong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9482387/
https://www.ncbi.nlm.nih.gov/pubmed/35946057
http://dx.doi.org/10.1002/mgg3.2030

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9482387/
https://www.ncbi.nlm.nih.gov/pubmed/35946057
http://dx.doi.org/10.1002/mgg3.2030

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