Co-creating a knowledge base in the "22q11.2 deletion syndrome" community. (2020)
Attributed to:
MRC Centre for Neuropsychiatric Genetics and Genomics
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1007/s12687-019-00425-8
PubMed Identifier: 31129779
Publication URI: http://europepmc.org/abstract/MED/31129779
Type: Journal Article/Review
Volume: 11
Parent Publication: Journal of community genetics
Issue: 1
ISSN: 1868-310X