检索结果 - 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 由 Klatt Regan EM, Bowdin Sarah C, Fenwick Aimee L, Wilkie Andrew OM

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

    出版 2012
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