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Pediatric clinical exome/genome sequencing and the engagement process: encouraging active conversation with the older child and adolescent: points to consider—a statement of the American College of Medical Genetics and Genomics (ACMG)
Genetics in Medicine ( IF 6.6 ) Pub Date : 2018-03-22 , DOI: 10.1038/gim.2018.36
Lynn W Bush 1 , Louis E Bartoshesky 2 , Karen L David 3 , Benjamin Wilfond 4 , Janet L Williams 5 , Ingrid A Holm 6 ,
Affiliation  

Disclaimer: This article is designed primarily as an educational resource for medical geneticists and other health care providers to help them provide quality patient care. Adherence to the information contained in this article does not necessarily assure a successful medical outcome. This information and any associated recommendations should not be considered inclusive of all proper procedures and tests or exclusive of other procedures and tests that are reasonably directed to obtaining the same results. In determining the propriety of any specific procedure or test, each provider should apply his or her own professional judgment to the specific clinical circumstances presented by the individual patient. It may be prudent, however, to document in the patient’s record the rationale for any significant deviation from the recommendations set forth in this article. This article is copyrighted and is property of the American College of Medical Genetics. All authors have filed conflict of interest statements with the American College of Medical Genetics. Any conflicts have been resolved through a process approved by the Board of Directors. The American College of Medical Genetics has neither solicited nor accepted any commercial involvement in the development of the content of this publication.

中文翻译:

儿科临床外显子组/基因组测序和参与过程:鼓励与年龄较大的儿童和青少年积极对话:需要考虑的要点——美国医学遗传学和基因组学学院 (ACMG) 的声明

免责声明:本文主要作为医学遗传学家和其他医疗保健提供者的教育资源,以帮助他们提供优质的患者护理。遵守本文中包含的信息并不一定能保证取得成功的医疗结果。此信息和任何相关建议不应被视为包括所有适当的程序和测试,或不包括合理地用于获得相同结果的其他程序和测试。在确定任何特定程序或测试的适当性时,每个提供者都应将他或她自己的专业判断应用于个别患者提出的特定临床情况。然而,这可能是谨慎的,在患者记录中记录与本文中提出的建议有任何重大偏差的理由。本文受版权保护,是美国医学遗传学学院的财产。所有作者都向美国医学遗传学学院提交了利益冲突声明。任何冲突均已通过董事会批准的程序解决。美国医学遗传学学院既没有征求也没有接受任何商业参与来开发本出版物的内容。
更新日期:2018-03-16
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