Informed consent process for patient participation in rare disease registries linked to biorepositories
Titel:
Informed consent process for patient participation in rare disease registries linked to biorepositories
Auteur:
Rubinstein, Yaffa R. Groft, Stephen C. Chandros, Sara Hull Kaneshiro, Julie Karp, Barbara Lockhart, Nicole C. Marshall, Patricia A. Moxley III, Richard T. Pollen, Geraldine B. Miller, Vanessa Rangel Schwartz, Jack