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OFCD syndrome and extraembryonic defects are revealed by conditional mutation of the Polycomb-group repressive complex 1.1 (PRC1.1) gene BCOR. (2020)

First Author: Hamline MY

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