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JMG.39.11.804
JMG.39.11.804
http://dx.doi.org/10.1136/JMG.39.11.804
De novo GLI3 mutation in acrocallosal syndrome: broadening the phenotypic spectrum of GLI3 defects and overlap with murine models
P356
Q24679687-18A1DBEF-E9C8-4412-A4FD-5521829D9364
P356
JMG.39.11.804
http://dx.doi.org/10.1136/JMG.39.11.804