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We must to improve variability observed about written inform consents and to promote advance directives in clinical decision making.
Written inform consent was obtained from each subject enrolled into the study [7].
According to the French law, written inform consent was not required for this type of study.
For all probands written inform consent was signed by the patients or parents or the legal representative.
Biopsies and colonic resection samples were obtained after a written inform consent from all the patients, as requested by the clinical guides of Hospital del Mar.
This study was approved by the local Institutional Review Board (IRB) and written inform consents were obtained for all participants of the study.
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All participants obtained written informed consent.
Provided written informed consent Exclusion criteria 1.
All subjects provided written, informed consent.
Participants' written informed consent was obtained.
The donors gave their written informed consent.
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