Search Results - Daire, V.C.

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    Crouzon syndrome and Bent bone dysplasia associated with mutations at the same Tyr-381 residue in FGFR2 gene

    Crouzon syndrome and Bent bone dysplasia associated with mutations at the same Tyr-381 residue in FGFR2 gene by Collet, C., Alessandri, J.-L., Arnaud, E., Balu, M., Daire, V.C., Di Rocco, F.

    Published in Clinical genetics
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