Search Results - Fenwick Aimée L

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    A deletion of <it>FGFR2 </it>creating a chimeric IIIb/IIIc exon in a child with Apert syndrome by Klatt Regan EM, Bowdin Sarah C, Fenwick Aimee L, Wilkie Andrew OM

    Published 2011
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    Frank-ter Haar syndrome associated with sagittal craniosynostosis and raised intracranial pressure by Bendon Charlotte L, Fenwick Aimée L, Hurst Jane A, Nürnberg Gudrun, Nürnberg Peter, Wall Steven A, Wilkie Andrew OM, Johnson David

    Published 2012
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