1 | MGORS1, ORC1
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| Deficiency in origin licensing proteins impairs cilia formation: implications for the aetiology of Meier-Gorlin syndrome.
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| Stiff T, Alagoz M, Alcantara D, Outwin E, Brunner HG, Bongers EM, O'Driscoll M, Jeggo PA.
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| PLoS Genet 9(3):e1003360. doi: 10.1371/journal.pgen.1003360. Epub 2013 Mar 14.
2013
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2 | MGORS1, ORC1
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| Meier-Gorlin syndrome mutations disrupt an Orc1 CDK inhibitory domain and cause centrosome reduplication.
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| Hossain M, Stillman B.
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| Genes Dev 26(16):1797-810. doi: 10.1101/gad.197178.112. Epub 2012 Aug 1.
2012
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3 | MGORS1, ORC1
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| The BAH domain of ORC1 links H4K20me2 to DNA replication licensing and Meier-Gorlin syndrome.
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| Kuo AJ, Song J, Cheung P, Ishibe-Murakami S, Yamazoe S, Chen JK, Patel DJ, Gozani O.
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| Nature 484(7392):115-9. doi: 10.1038/nature10956.
2012
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4 | MGORS1, ORC1
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| Mutations in ORC1, encoding the largest subunit of the origin recognition complex, cause microcephalic primordial dwarfism resembling Meier-Gorlin syndrome.
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| 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.
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| Nat Genet 43(4):350-5.
2011
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5 | EPSS, MGORS1, MGORS3, MGORS4, MGORS5
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| Meier-Gorlin syndrome: report of eight additional cases and review.
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| 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.
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| Am J Med Genet 102(2):115-24. Review.
2001
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