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

出版年份 2020 全文链接

标题

作者

关键词

Oculofaciocardiodental syndrome, Craniofacial, Cardiac, X-linked developmental disorder, Salivary glands, Placenta

出版物

Volume -, Issue -, Pages -

出版商

Elsevier BV

发表日期

2020-07-18

DOI

10.1016/j.ydbio.2020.06.013

联系作者

Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.

Explore

Do you already have a recorded webinar? Grow your audience and get more views by easily listing your recording on Peeref.

Upload Now