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302245
302245
http://dx.doi.org/10.1086/302245
De novo alu-element insertions in FGFR2 identify a distinct pathological basis for Apert syndrome
P356
Q34388821-5A362024-ADB5-4E51-99C9-390D58C231B9
P356
302245
http://dx.doi.org/10.1086/302245