Hajihosseini, Mohammad K., Wilson, Stephen, De Moerlooze, Laurence and Dickson, Clive (2001) A splicing switch and gain-of-function mutation in FgfR2-IIIc hemizygotes causes Apert/Pfeiffer-syndrome-like phenotypes. Proceedings of the National Academy of Sciences, 98 (7). pp. 3855-3860. ISSN 0027-8424
Full text not available from this repository.| Item Type: | Article |
|---|---|
| Faculty \ School: | Faculty of Science > School of Biological Sciences |
| UEA Research Groups: | Faculty of Science > Research Groups > Cells and Tissues |
| Depositing User: | EPrints Services |
| Date Deposited: | 01 Oct 2010 13:37 |
| Last Modified: | 25 Sep 2026 14:46 |
| URI: | https://uea-test-2026.eprints-hosting.org/id/eprint/843 |
| DOI: | 10.1073/pnas.071586898 |
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