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J.DEVCEL.2005.12.003
J.DEVCEL.2005.12.003
http://dx.doi.org/10.1016/J.DEVCEL.2005.12.003
Crkl deficiency disrupts Fgf8 signaling in a mouse model of 22q11 deletion syndromes.
P356
Q35606917-3413F6B8-6537-4A49-84DA-BD4AC8472712
P356
J.DEVCEL.2005.12.003
http://dx.doi.org/10.1016/J.DEVCEL.2005.12.003