Genetic aetiology distribution of 398 foetuses with congenital heart disease in the prenatal setting

AIMS: Copy number variant‐sequencing (CNV‐seq) and exome sequencing (ES) have been used as powerful tools in understanding the role of genetic variants in congenital heart diseases (CHDs). A few previous large cohort studies have utilized CNV‐seq and ES to investigate prenatally diagnosed CHD. Here,...

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Detalles Bibliográficos
Autores principales: Yi, Tong, Hao, Xiaoyan, Sun, Hairui, Zhang, Ye, Han, Jiancheng, Gu, Xiaoyan, Sun, Lin, Liu, Xiaowei, Zhao, Ying, Guo, Yong, Zhou, Xiaoxue, He, Yihua
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/PMC10053168/
https://www.ncbi.nlm.nih.gov/pubmed/36478645
http://dx.doi.org/10.1002/ehf2.14209

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10053168/
https://www.ncbi.nlm.nih.gov/pubmed/36478645
http://dx.doi.org/10.1002/ehf2.14209

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