DOI:
10.1055/s-00029027
Journal of Pediatric Genetics
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References
Horn D, Kapeller J, Rivera-Brugués N. , et al.
Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits.
Hum Mutat 2010;
31 (11) E1851-E1860
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