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Human subject approval was sought and received from Essentia Health's Institutional Review Board IRBB).
This study was performed after human subject approval from the Karolinska Hospital.
Primary CLL specimens analyzed in this study were obtained from untreated CLL patients after appropriate human subject approval.
Human subject approval from the University of Michigan was obtained to use residual amniocentesis samples that were to be discarded.
Human subject approval was obtained from the institutional review boards (IRB) of M.D. Anderson Cancer Center, Baylor College of Medicine and Kelsey-Seybold Clinics.
The protocol was approved by the Type 1 Diabetes TrialNet Steering Committee, the Data and Safety Monitoring Board (DSMB), and regulatory authorities; human subject approval was obtained at participating sites prior to study initiation.
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Human subject approvals were obtained from institutional review boards at all participating institutions.
Human subject approvals were obtained from the Institutional Review Boards at all of the SPUR-Net constituent organizations.
Thus, the current manuscript adheres to appropriate exclusions from human subjects approval.
Human subjects' approval was gained from the Medical Ethic Committee of Harbin Medical University.
The Saint Louis University Institutional Review Board reviewed and granted human subjects approval.
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