A splicing switch and gain-of-function mutation in FgfR2-IIIc hemizygotes causes Apert/Pfeiffer-syndrome-like phenotypes

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

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Item Type: Article
Faculty \ School: Faculty of Science > School of Biological Sciences
Depositing User: EPrints Services
Date Deposited: 01 Oct 2010 13:37
Last Modified: 24 Jul 2019 17:37
URI: https://ueaeprints.uea.ac.uk/id/eprint/843
DOI: 10.1073/pnas.071586898

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