Prenatal genetic diagnosis of omphalocele by karyotyping, chromosomal microarray analysis and exome sequencing
Author:
Affiliation:
1. Gentic Medical Center, Guangdong Women and Children Hospital, Guangzhou, PR China
Funder
Traditional Chinese Medicine Bureau of Guangdong Province, China
Publisher
Informa UK Limited
Subject
General Medicine
Link
https://www.tandfonline.com/doi/pdf/10.1080/07853890.2021.1962966
Reference17 articles.
1. The outcomes of pregnancies following a prenatal diagnosis of fetal exomphalos in Western Australia
2. Prenatal diagnosis and management of omphalocele
3. Omphalocele—What should we tell the prospective parents?
4. Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study
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