DOI: 10.1055/s-00029027

Journal of Pediatric Genetics

References

Palumbo O, D'Agruma L, Minenna AF. , et al.
3p14.1 de novo microdeletion involving the FOXP1 gene in an adult patient with autism, severe speech delay and deficit of motor coordination.

Gene 2013;
516 (01) 107-113

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