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Research Article
Presence of the Apert canonical S252W FGFR2 mutation in a patient without severe syndactyly.

Authors

    Citation

    Passos-Bueno MR, Richieri-Costa A, Sertié AL, et al
    Presence of the Apert canonical S252W FGFR2 mutation in a patient without severe syndactyly.
    Journal of Medical Genetics 1998;35:677-679.

    Publication history

    • First published August 1, 1998.
    Online issue publication 
    April 27, 2016

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