Ready or not, genomic screening of fetuses is already here
Author:
Funder
National Institutes of Health
National Human Genome Research Institute
Publisher
Elsevier BV
Subject
Genetics (clinical)
Reference12 articles.
1. Diagnostic yield of exome sequencing for prenatal diagnosis of fetal structural anomalies: a systematic review and meta-analysis;Mellis;Prenat Diagn,2022
2. High rate of abnormal findings in prenatal exome trio in low risk pregnancies and apparently normal fetuses;Vaknin;Prenat Diagn,2022
3. International Society for prenatal diagnosis 2022 debate 3-fetal genome sequencing should be offered to all pregnant patients;Van den Veyver;Prenat Diagn,2023
4. International Society for prenatal diagnosis updated Position Statement on the use of genome-wide sequencing for prenatal diagnosis;Van den Veyver;Prenat Diagn,2022
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