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Bicknell, Louise S, Walker, Sarah, Klingseisen, Anna, Stiff, Tom, Leitch, Andrea, Kerzendorfer, Claudia, Martin, Carol-Anne, Yeyati, Patricia, Al Sanna, Nouriya, Bober, Michael, Johnson, Diana, Wise, Carol, Jackson, Andrew P, O'Driscoll, Mark and Jeggo, Penny A (2011) Mutations in ORC1, encoding the largest subunit of the origin recognition complex, cause microcephalic primordial dwarfism resembling Meier-Gorlin syndrome. Nature Genetics, 43 (4). pp. 350-355. ISSN 1061-4036
Full text not available from this repository.
Official URL: http://dx.doi.org/10.1038/ng.776
Item Type: | Article |
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Additional Information: | This article was featured on the journal cover. |
Schools and Departments: | School of Life Sciences > Sussex Centre for Genome Damage and Stability |
Subjects: | Q Science |
Depositing User: | Sarah Walker |
Date Deposited: | 06 Feb 2012 19:38 |
Last Modified: | 26 Jun 2013 09:00 |
URI: | http://sro.sussex.ac.uk/id/eprint/21606 |