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000368865
000368865
http://dx.doi.org/10.1159/000368865
A mouse splice-site mutant and individuals with atypical chromosome 22q11.2 deletions demonstrate the crucial role for crkl in craniofacial and pharyngeal development.
P356
Q34800084-ABBE63DD-60D2-49A6-9810-53CBE0E77E86
P356
000368865
http://dx.doi.org/10.1159/000368865