OBO ID: DOID:0060306

Citations

(3 total)

Term: Meier-Gorlin syndrome

Maerz, L.D., Casar Tena, T., Gerhards, J., Donow, C., Jeggo, P.A., Philipp, M. (2019) Analysis of cilia dysfunction phenotypes in zebrafish embryos depleted of Origin recognition complex factors. European journal of human genetics : EJHG. 27(5):772-782

Yao, L., Chen, J., Wu, X., Jia, S., Meng, A. (2017) Zebrafish cdc6 hypomorphic mutation causes Meier-Gorlin syndrome-like phenotype. Human molecular genetics. 26(21):4168-4180

Kuo, A.J., Song, J., Cheung, P., Ishibe-Murakami, S., Yamazoe, S., Chen, J.K., Patel, D.J., and Gozani, O. (2012) The BAH domain of ORC1 links H4K20me2 to DNA replication licensing and Meier-Gorlin syndrome. Nature. 484(7392):115-119