Ethical Considerations of Genome Sequencing for Pediatric Patients
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Pediatrics, Perinatology and Child Health
Reference19 articles.
1. Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test;Lionel;Genet Med,2018
2. Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology;Richards;Genet Med,2015
3. Reporting incidental findings in genomic scale clinical sequencing–a clinical laboratory perspective: a report of the Association for Molecular Pathology;Hegde;J Mol Diagn,2015
4. Actionable exomic incidental findings in 6503 participants: challenges of variant classification;Amendola;Genome Res,2015
5. Ethical issues in newborn sequencing research: the case study of BabySeq;Ross;Pediatrics,2019
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Incidental finding at methylation-specific multiplex ligation-dependent probe amplification (MS-MLPA): how to proceed?;Frontiers in Genetics;2023-10-03
2. Pediatric Neuroethics: Current Controversies with Timeless Reasoning;Seminars in Pediatric Neurology;2023-04
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