Citations for
1MGORS1, ORC1
Deficiency in origin licensing proteins impairs cilia formation: implications for the aetiology of Meier-Gorlin syndrome.
Stiff T, Alagoz M, Alcantara D, Outwin E, Brunner HG, Bongers EM, O'Driscoll M, Jeggo PA.
PLoS Genet 9(3):e1003360. doi: 10.1371/journal.pgen.1003360. Epub 2013 Mar 14. 2013
2MGORS1, ORC1
Meier-Gorlin syndrome mutations disrupt an Orc1 CDK inhibitory domain and cause centrosome reduplication.
Hossain M, Stillman B.
Genes Dev 26(16):1797-810. doi: 10.1101/gad.197178.112. Epub 2012 Aug 1. 2012
3MGORS1, ORC1
The BAH domain of ORC1 links H4K20me2 to DNA replication licensing and Meier-Gorlin syndrome.
Kuo AJ, Song J, Cheung P, Ishibe-Murakami S, Yamazoe S, Chen JK, Patel DJ, Gozani O.
Nature 484(7392):115-9. doi: 10.1038/nature10956. 2012
4MGORS1, ORC1
Mutations in ORC1, encoding the largest subunit of the origin recognition complex, cause microcephalic primordial dwarfism resembling Meier-Gorlin syndrome.
Bicknell LS, Walker S, Klingseisen A, Stiff T, Leitch A, Kerzendorfer C, Martin CA, Yeyati P, Al Sanna N, Bober M, Johnson D, Wise C, Jackson AP, O'Driscoll M, Jeggo PA.
Nat Genet 43(4):350-5. 2011
5EPSS, MGORS1, MGORS3, MGORS4, MGORS5
Meier-Gorlin syndrome: report of eight additional cases and review.
Bongers EM, Opitz JM, Fryer A, Sarda P, Hennekam RC, Hall BD, Superneau DW, Harbison M, Poss A, van Bokhoven H, Hamel BC, Knoers NV.
Am J Med Genet 102(2):115-24. Review. 2001