Skip to Main Content

Paper Details

Practical guidance on informed consent for pediatric participants in a biorepository.
Mayo Clin Proc
21
2014
participants, pediatric
Adolescent, Biological Specimen Banks, Child, Child Welfare, Genetic Research, Guidelines as Topic, Humans, Informed Consent, National Human Genome Research Institute (U.S.), Parental Consent, Specimen Handling, United States
Author NameAffiliation
Kyle B BrothersUniversity of Louisville School of Medicine
John LynchUniversity of Cincinnati
Sharon AufoxCenter for Genetic Medicine, Northwestern University Feinberg School of Medicine
John J ConnollyCenter for Applied Genomics, Children's Hospital of Philadelphia
Bruce D GelbMindich Child Health and Development Institute, Icahn School of Medicine at Mount Sinai
Bruce D GelbMindich Child Health and Development Institute, Icahn School of Medicine at Mount Sinai
Ingrid A HolmDivision of Genetics and Genomics and The Manton Center for Orphan Disease Research, Boston Children's Hospital, and Harvard Medical School
Ingrid A HolmDivision of Genetics and Genomics and The Manton Center for Orphan Disease Research, Boston Children's Hospital, and Harvard Medical School
Saskia C SandersonIcahn School of Medicine at Mount Sinai
Jennifer B McCormickDivisions of General Internal Medicine and Health Care and Policy Research and the Mayo Biomedical Ethics Program, Mayo Clinic
Janet L WilliamsGenomic Medicine Institute
Wendy A WolfBoston Children's Hospital
Armand H Matheny AntommariaCincinnati Children's Hospital Medical Center
E ClaytonCenter for Biomedical Ethics and Society, Vanderbilt University Medical Center
  • 1 - 14

Datasets