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
UEA Research Groups:	Faculty of Science > Research Groups > Cells and Tissues
Depositing User:	EPrints Services
Date Deposited:	01 Oct 2010 13:37
Last Modified:	22 Apr 2023 23:45
URI:	https://ueaeprints.uea.ac.uk/id/eprint/843
DOI:	10.1073/pnas.071586898

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