Can children and young people consent to be tested for adult onset genetic disorders? Commentary: Weighing burdens and benefits rather than competence
Author:
Publisher
BMJ
Subject
General Earth and Planetary Sciences,General Environmental Science,General Engineering
Cited by 25 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. The future of newborn screening for lysosomal disorders;Neuroscience Letters;2021-08
2. Defining the Clinical Value of a Genomic Diagnosis in the Era of Next-Generation Sequencing;Annual Review of Genomics and Human Genetics;2016-08-31
3. Predictive genetic testing in minors for late-onset conditions: a chronological and analytical review of the ethical arguments: Figure 1;Journal of Medical Ethics;2012-03-08
4. “You're one of us now”: Young people describe their experiences of predictive genetic testing for Huntington disease (HD) and familial adenomatous polyposis (FAP);American Journal of Medical Genetics Part C: Seminars in Medical Genetics;2008
5. Maturity of judgement in decision making for predictive testing for nontreatable adult-onset neurogenetic conditions: a case against predictive testing of minors;Clinical Genetics;2006-09-06
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