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

Hamline MY, Corcoran CM, Wamstad JA, Miletich I, Feng J, Lohr JL, Hemberger M, Sharpe PT, Gearhart MD, Bardwell VJ
Dev Biol. 2020 Dec 1;468(1-2):110-132. doi: 10.1016/j.ydbio.2020.06.013. Epub 2020 Jul 18. PubMed Article

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