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A mouse splice-site mutant and individuals with atypical chromosome 22q11.2 deletions demonstrate the crucial role for crkl in craniofacial and pharyngeal development.

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author: Susan White  Kerry Miller  John F. Bertram  John F. Bateman  Zornitza Stark  Tiong Y Tan  Peter G Farlie  Ravi Savarirayan 

Publication date November 8, 2014
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