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This study protocol was approved by the ethics committee of our hospital, and informed consent was obtained from enrolled patients.
All human blood samples were obtained from enrolled individuals with the approval of institutional review board at the University of Florida.
All human blood samples were obtained from enrolled individuals with the approval of the institutional review board (IRB) at the University of Florida.
Written informed consent was obtained from enrolled adults and the Research Ethics Committee of the University of Cape Town approved this study (REC 178/2008).
Stool samples obtained from enrolled children were tested for enteric viruses.
Samples of endometrial tissue and uterine flushing were obtained from enrolled subjects after obtaining their informed consent.
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Additional samples were obtained from men enrolled on chemotherapy trials.
Written informed consent was obtained from all enrolled patients.
Written informed consent was obtained from all enrolled study participants.
Strains and specimens used in this study were obtained from patients enrolled in different studies.
Specimens were obtained from subjects enrolled in an observational study registered with ClinicalTrials.gov as NCT00281229.
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