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Fig. 4 | Molecular Autism

Fig. 4

From: Prospective investigation of FOXP1 syndrome

Fig. 4

Dysmorphisms in individuals with FOXP1 mutations. Most common features include prominent forehead (evident in a, b, c, d, g, and h), bulbous nose (evident in a, c, e, f, g, and h), broad nasal bridge (evident in a, b, c, e, and h), hypertelorism (evident in a, c, and h), thick vermillion (evident in e, f, and h), and long philtrum (evident in c and g)

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