Lessons learnt from prenatal exome sequencing
Author:
Affiliation:
1. North Thames Genomic Laboratory Hub Great Ormond Street Hospital for Children NHS Foundation Trust London UK
2. Genetics and Genomic Medicine UCL Great Ormond Street Institute of Child Health London UK
Publisher
Wiley
Subject
Genetics (clinical),Obstetrics and Gynecology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/pd.6165
Reference34 articles.
1. Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study
2. Whole exome sequencing as a diagnostic adjunct to clinical testing in fetuses with structural abnormalities
3. Promises, pitfalls and practicalities of prenatal whole exome sequencing
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1. Fetal whole genome sequencing as a clinical diagnostic tool: Advantages, limitations and pitfalls;Best Practice & Research Clinical Obstetrics & Gynaecology;2024-12
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3. Potentially Missed Diagnoses in Prenatal Versus Postnatal Exome Sequencing in the Lack of Informative Phenotype: Lessons Learned From a Postnatal Cohort;Prenatal Diagnosis;2024-09-05
4. Current status and future of genomics in fetal and maternal medicine: A scientific review commissioned by European Board and College of Obstetrics and Gynaecology (EBCOG);European Journal of Obstetrics & Gynecology and Reproductive Biology;2024-08
5. Delivery of a national prenatal exome sequencing service in England: a mixed methods study exploring healthcare professionals’ views and experiences;Frontiers in Genetics;2024-06-05
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