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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1. Guidelines for NGS procedures applied to prenatal diagnosis by the Spanish Society of Gynecology and Obstetrics and the Spanish Association of Prenatal Diagnosis;Journal of Medical Genetics;2024-06-04
2. Attitudes toward uncertain results from prenatal exome sequencing: a national survey among healthcare professionals working in the prenatal setting;Frontiers in Medicine;2024-05-15
3. The incremental yield of prenatal exome sequencing over chromosome microarray for congenital heart abnormalities: A systematic review and meta‐analysis;Prenatal Diagnosis;2024-05-06
4. ‘Something that helped the whole picture’: Experiences of parents offered rapid prenatal exome sequencing in routine clinical care in the English National Health Service;Prenatal Diagnosis;2024-03-05
5. Clinical Experience of Prenatal Chromosomal Microarray Analysis in 6159 Ultrasonically Abnormal Fetuses;Reproductive Sciences;2023-11-27
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