Return of results to the families of children in genomic sequencing: Tallying risks and benefits

Genetics in Medicine

Volumn 15, Issue 6, 2013, Pages 435-436

  Evans, James P ^a  

^a UNIVERSITY OF NORTH CAROLINA SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ABNORMAL LABORATORY RESULT; CHILD HEALTH CARE; CLINICAL MEDICINE; EDITORIAL; FAMILY HISTORY; GENE MUTATION; GENE SEQUENCE; GENETIC RISK; GENETIC SCREENING; GENOMICS; HUMAN; INCIDENTAL FINDING; MATERNAL CARE; PATIENT AUTONOMY; PSYCHOLOGICAL ASPECT; REPRODUCIBILITY; RISK BENEFIT ANALYSIS;

EID: 84878862598     PISSN: 10983600     EISSN: 15300366     Source Type: Journal    
DOI: 10.1038/gim.2013.54     Document Type: Editorial

References (2)

1. Friedman Ross L, Salls HM, David KL, Anderson RR. Technical report: ethical and policy issues in genetic testing and screening of children. Genet Med 2013;15:234-245.
2. A merican College of Medical Genetics and Genomics. ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing. http://www.acmg.net/docs/ACMG-Releases-Highly-Anticipated-Recommendations-on- Incidental-Findings-in-Clinical-Exome-and-Genome-Sequencing.pdf. 19 March 2013.