Author:
Ashton-Prolla Patrícia,Goldim José Roberto,Vairo Filippo Pinto e,da Silveira Matte Ursula,Sequeiros Jorge
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Public Health, Environmental and Occupational Health,Epidemiology
Reference79 articles.
1. ACMG (American College of Medical Genetics) Board of Directors (2013) Points to consider for informed consent for genome/exome sequencing. Genet Med 15:748–749
2. Abul-Husn NS, Owusu Obeng A, Sanderson SC et al (2014) Implementation and utilization of genetic testing in personalized medicine. Pharm Pers Med 13:227–240. doi: 10.2147/PGPM.S48887. eCollection 2014
3. Annas GJ, Elias S (2014) 23andMe and the FDA. N Engl J Med 370:985–988. doi: 10.1056/NEJMp1316367
4. ANS (2013) Anex of Document 876/GGRAS/DIPRO/ANS of Dec 4th 2013. Available at http://www.ans.gov.br/images/stories/noticias/pdf/anexo%20nota%20tcnica%20analise%20molecular%20de%20dna.pdf . Accessed 25 May 2015
5. Apellániz-Ruiz M, Lee MY, Sánchez-Barroso L, Gutiérrez-Gutiérrez G, Calvo I, García-Estévez L, Sereno M, García-Donás J, Castelo B, Guerra E, Leandro-García LJ, Cascón A, Johansson I, Robledo M, Ingelman-Sundberg M, Rodríguez-Antona C (2015) Whole-exome sequencing reveals defective CYP3A4 variants predictive of paclitaxel dose-limiting neuropathy. Clin Cancer Res 21(2):322–328. doi: 10.1158/1078-0432.CCR-14-1758
Cited by
18 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