Evidence to Support the Clinical Utility of Prenatal Exome Sequencing in Evaluation of the Fetus with Congenital Anomalies
Author:
Publisher
Wiley
Subject
Obstetrics and Gynecology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/1471-0528.16616
Reference29 articles.
1. Exome sequencing in the assessment of congenital malformations in the fetus and neonate;Mone F;Arch Dis Child Fetal Neonatal Ed,2019
2. Promises, pitfalls and practicalities of prenatal whole exome sequencing
3. Genome-Wide Sequencing for Prenatal Detection of Fetal Single-Gene Disorders
4. Clinical Whole-Exome Sequencing for the Diagnosis of Mendelian Disorders
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2. Diagnostic yield of prenatal exome sequencing in the genetic screening of fetuses with brain anomalies detected by MRI and ultrasonography: A systematic review and meta‐analysis;BJOG: An International Journal of Obstetrics & Gynaecology;2023-11-06
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4. Systematic evaluation of genome sequencing for the diagnostic assessment of autism spectrum disorder and fetal structural anomalies;The American Journal of Human Genetics;2023-09
5. Copy number variants and fetal structural abnormalities in stillborn fetuses: A secondary analysis of the Stillbirth Collaborative Research Network study;BJOG: An International Journal of Obstetrics & Gynaecology;2023-06
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