Parental experiences of rapid exome sequencing in cases with major ultrasound anomalies during pregnancy-Reference-Cited by-同舟云学术

Parental experiences of rapid exome sequencing in cases with major ultrasound anomalies during pregnancy

Published:2021-10-22 Issue: Volume: Page:
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenatal Diagnosis

Author:

Plantinga Mirjam¹^ORCID,Zwienenberg Lauren¹,Dijk Eva¹,Breet Hanna¹,Diphoorn Janouk¹,El Mecky Julia¹²,Bouman Katelijne¹,Verheij Joke¹,Birnie Erwin¹,Ranchor Adelita V.³,Corsten‐Janssen Nicole¹^ORCID,Langen Irene M.¹

Affiliation:

1. Department of Genetics University Medical Center Groningen University of Groningen Groningen The Netherlands

2. Clinical Ethics and Law, Faculty of Medicine University of Southampton Southampton UK

3. Department of Health Psychology University Medical Center Groningen University of Groningen Groningen The Netherlands

Funder

Universitair Medisch Centrum Groningen

Publisher

Wiley

Subject

Genetics(clinical),Obstetrics and Gynaecology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/pd.6056

Reference24 articles.

1. Promises, pitfalls and practicalities of prenatal whole exome sequencing;Best S;Prenat Diagn,2018

2. Identifying the genetic causes for prenatally diagnosed structural congenital anomalies (SCAs) by whole‐exome sequencing (WES);Leung G;BMC Med Genom,2018

3. Application of exome sequencing for prenatal diagnosis: a rapid scoping review;Pratt M;Genet Med,2020

4. The use of fetal exome sequencing in prenatal diagnosis: a points to consider document of the American College of Medical Genetics and Genomics (ACMG);Monaghan KG;Genet Med,2020

5. Scanning the body, sequencing the genome: dealing with unsolicited findings;Wouters RHP;Bioethics,2017

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1. ‘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

2. Hope, but never expect? Comparing parents' pre‐ and post‐disclosure attitudes toward return of results from diagnostic exome sequencing for their child;Molecular Genetics & Genomic Medicine;2024-02-17

3. Ethics of artificial intelligence in prenatal and pediatric genomic medicine;Journal of Community Genetics;2023-10-05

4. Access to prenatal exome sequencing for fetal malformations: A qualitative landscape analysis in the US;Prenatal Diagnosis;2023-09-26

5. Prenatal diagnosis to identify compound heterozygous variants in PKDCC that causes rhizomelic limb shortening with dysmorphic features in a fetus from China;BMC Medical Genomics;2023-08-17