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Raffan, Eleanor, Hurst, Liam A, Al Turki, Saeed, Carpenter, Gillian, Scott, Carol, Daly, Allan, Coffey, Alison, Bhaskar, Sanjeev, Howard, Eleanor, Khan, Naz, Kingston, Helen, Palotie, Aarno, Savage, David B, O'Driscoll, Mark, Smith, Claire, O'Rahilly, Stephen, Barroso, Inês and Semple, Robert K (2011) Early diagnosis of Werner's syndrome using exome-wide sequencing in a single, atypical patient. Frontiers in Genomic Endocrinology, 2 (Articl).
Full text not available from this repository.
Official URL: http://dx.doi.org/10.3389/fendo.2011.00008
Item Type: | Article |
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Additional Information: | This was the first article to be published in the inaugural issue of this journal. |
Schools and Departments: | School of Life Sciences > Sussex Centre for Genome Damage and Stability |
Depositing User: | Gillian Carpenter |
Date Deposited: | 06 Feb 2012 18:35 |
Last Modified: | 30 Nov 2012 17:00 |
URI: | http://srodev.sussex.ac.uk/id/eprint/17255 |