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Norwegian Childhood Cancer Biobank
NCCB
Data Resource:  NCCB
Point of Contact:  
Monica C. Munthe-Kaas,  
Project

About This Dataset
The childhood cancer biobanking started at Oslo University Hospital in March 2017 and was from 2019 run as a national Norwegian Childhood Cancer Biobank. Informed consent and biological samples are collected regionally and stored centrally. Approximately 12,000 samples from 510 patients and have been included by January 1, 2021, representing a 96% consent and participation rate among our newly diagnosed patients.
Core Data Elements
Additional Data Elements
DATA REPOSITORY
Published In
https://doi.org/10.1002/cnr2.1555