Rare De Novo Copy Number Variants in Patients with Congenital Pulmonary Atresia

BACKGROUND: Ongoing studies using genomic microarrays and next-generation sequencing have demonstrated that the genetic contributions to cardiovascular diseases have been significantly ignored in the past. The aim of this study was to identify rare copy number variants in individuals with congenital...

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Detalles Bibliográficos
Autores principales: Xie, Li, Chen, Jin-Lan, Zhang, Wei-Zhi, Wang, Shou-Zheng, Zhao, Tian-Li, Huang, Can, Wang, Jian, Yang, Jin-Fu, Yang, Yi-Feng, Tan, Zhi-Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4020819/
https://www.ncbi.nlm.nih.gov/pubmed/24826987
http://dx.doi.org/10.1371/journal.pone.0096471

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4020819/
https://www.ncbi.nlm.nih.gov/pubmed/24826987
http://dx.doi.org/10.1371/journal.pone.0096471

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