Apert syndrome with S252W FGFR2 mutation and characterization using Phenomizer: An Indian case report (Q38435762)

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scientific article published on 13 July 2016
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Apert syndrome with S252W FGFR2 mutation and characterization using Phenomizer: An Indian case report
scientific article published on 13 July 2016

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    Apert syndrome with S252W FGFR2 mutation and characterization using Phenomizer: An Indian case report (English)
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    13 July 2016
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