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Results 1 - 4 of 4 for "Meier-Gorlin" syndrome 8
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  1. ORC6 gene 
    ... I, Nogales E, Botchan MR, Berger JM. A Meier-Gorlin syndrome mutation in a conserved C-terminal helix of Orc6 impedes origin recognition complex formation. Elife. 2013 Oct 8;2:e00882. doi: 10.7554/eLife.00882. Citation ...
    https://medlineplus.gov/genetics/gene/orc6 - Genetics
  2. ORC1 gene 
    ... S A. 2010 Aug 24;107(34):15093-8. doi: 10.1073/pnas.1009945107. Epub 2010 Aug ... aetiology of Meier-Gorlin syndrome. PLoS Genet. 2013;9(3):e1003360. doi: 10. ...
    https://medlineplus.gov/genetics/gene/orc1 - Genetics
  3. ORC4 gene 
    ... on heterochromatin. Mutations in the ORC4 gene cause Meier-Gorlin syndrome, a condition characterized by short stature, underdeveloped kneecaps, ... how a reduction in replication licensing leads to Meier-Gorlin syndrome. Researchers speculate that such a reduction delays the ...
    https://medlineplus.gov/genetics/gene/orc4 - Genetics
  4. CDT1 gene 
    ... to divide. Mutations in the CDT1 gene cause Meier-Gorlin syndrome, a condition characterized by short stature, underdeveloped kneecaps, ... how a reduction in replication licensing leads to Meier-Gorlin syndrome. Researchers speculate that such a reduction delays the ...
    https://medlineplus.gov/genetics/gene/cdt1 - Genetics