OFCD syndrome and extraembryonic defects are revealed by conditional mutation of the Polycomb-group repressive complex 1.1 (PRC1.1) gene BCOR. (2020)
Attributed to:
Wnt signalling and stem cell mobilisation in tissue injury repair
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1016/j.ydbio.2020.06.013
PubMed Identifier: 32692983
Publication URI: http://europepmc.org/abstract/MED/32692983
Type: Journal Article/Review
Volume: 468
Parent Publication: Developmental biology
Issue: 1-2
ISSN: 0012-1606