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CGE.12213
CGE.12213
http://dx.doi.org/10.1111/CGE.12213
Crouzon syndrome and Bent bone dysplasia associated with mutations at the same Tyr-381 residue in FGFR2 gene.
P356
Q43500408-31395C4E-E98F-421C-822C-3BFD45E7D85A
P356
CGE.12213
http://dx.doi.org/10.1111/CGE.12213