OFCD syndrome and extraembryonic defects are revealed by conditional mutation of the polycomb-group repressive complex 1.1 (PRC1.1) gene BCOR
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| Description | scientific article published on 18 July 2020 |
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author: Micah D Gearhart Myriam Hemberger Connie M. Corcoran Michelle Y. Hamline Vivian J. Bardwell Joseph A Wamstad |
| Publication date | July 18, 2020 |
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