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Informed consent was obtained from parents and teachers taking part; and assent was obtained from participating young children.
Clinical specimens were collected after verbal assent was obtained from participants younger than 12 years old or written informed consent from participants aged 12 years and older.
Assent was obtained from each child at 11 years.
Written informed consent or assent was obtained from all subjects.
Parental consent and students' assent was obtained, as well as an IRB approval.
Informed consent, or assent, was obtained from the patient or available next of kin.
Patient's informed consent or next of kin assent was obtained before inclusion whenever possible.
Written informed consent or assent was obtained from all the subjects.
Assent was obtained from all participants under 18 years.
Additional verbal assent was obtained from children 6 to 18 years of age.
Written assent was obtained from children in accordance with specific institutional practice.
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