Consent for samples used in this study was obtained in accordance with the Declaration of Helsinki on protocols that were reviewed and approved by the IRBs of MDACC or Dana-Farber/Harvard Cancer Center.
The research protocols for this study were approved by the institutional review boards (IRBs) of the University at Buffalo, University of Oklahoma Health Sciences Center and Seattle Children's Medical Center.
The study protocols, procedures, and consent statements were approved by the Institutional Review Boards (IRBs) of each participating site.
This study was approved by the Institutional Review Boards (IRBs) of the University of Kansas, HINU, and Johnson County Community College.
GPS' relevant education includes an M.A. Anthropology (with an emphasis on population genetics), an M.A. Philosophy, and a J.D. This study was approved by the Institutional Review Boards (IRBs) of the University of Kansas, HINU, and Johnson County Community College.
Human subjects research protocols for the LongROAD study were developed collaboratively by the investigators and were reviewed and approved individually by the institutional review boards (IRBs) of the participating institutions.
Institutional Review Board and Ethics: All of the data collected and analyzed received approval from the IRBs of PMH, the Botswana Ministry of Health, the University of Botswana, and PM's US home institution.
The Minnesota and Wisconsin IRBs of record concurred.
The IRBs of both universities approved the described studies.
This study was approved by the Institutional Review Boards (IRBs) of Johns Hopkins and Sinai Hospitals.
The research was approved by the IRBs of each participating institution and written consent was obtained for all participants.
