Prenatal genetic diagnosis of omphalocele by karyotyping, chromosomal microarray analysis and exome sequencing

OBJECTIVES: The aim of this study is to share our experience in the prenatal diagnosis of omphalocele by karyotyping, chromosomal microarray analysis (CMA) and whole exome sequencing (WES). METHODS: In this retrospective study, 81 cases of omphalocele were identified from 2015 to 2020. Associated an...

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Detalles Bibliográficos
Autores principales: Shi, Xiaomei, Tang, Hui, Lu, Jian, Yang, Xiue, Ding, Hongke, Wu, Jing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2021
Materias:
Medical Genetics & Genomics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8366676/
https://www.ncbi.nlm.nih.gov/pubmed/34374610
http://dx.doi.org/10.1080/07853890.2021.1962966

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8366676/
https://www.ncbi.nlm.nih.gov/pubmed/34374610
http://dx.doi.org/10.1080/07853890.2021.1962966

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