标题
Adolescent and parent perspectives on genomic sequencing to inform cancer care
作者
关键词
-
出版物
PEDIATRIC BLOOD & CANCER
Volume 69, Issue 9, Pages -
出版商
Wiley
发表日期
2022-06-23
DOI
10.1002/pbc.29791
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Patients’ and Oncologists’ Knowledge and Expectations Regarding Tumor Multigene Next‐Generation Sequencing: A Narrative Review
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- Adolescent and Young Adult Cancer Patients’ Experiences With Treatment Decision-making
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- Clinician‐patient‐family decision‐making and health literacy in adolescents and young adults with cancer and their families: A systematic review of qualitative studies
- (2019) Danielle Gessler et al. PSYCHO-ONCOLOGY
- Pediatric cancer families’ participation in whole-genome sequencing research in Denmark: Parent perspectives
- (2018) Anna Byrjalsen et al. EUROPEAN JOURNAL OF CANCER CARE
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- Toward Personalized Targeted Therapeutics: An Overview
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- Attitudes of parents toward the return of targeted and incidental genomic research findings in children
- (2014) Conrad V. Fernandez et al. GENETICS IN MEDICINE
- “It was the missing piece”: adolescent experiences of predictive genetic testing for adult-onset conditions
- (2013) Cara Mand et al. GENETICS IN MEDICINE
- Effects of informed consent for individual genome sequencing on relevant knowledge
- (2012) KA Kaphingst et al. CLINICAL GENETICS
- Social Networkers' Attitudes Toward Direct-to-Consumer Personal Genome Testing
- (2009) Amy L. McGuire et al. AMERICAN JOURNAL OF BIOETHICS
- Providing Research Results to Participants: Attitudes and Needs of Adolescents and Parents of Children With Cancer
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- Genetic testing in familial melanoma: uptake and implications
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