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Magnetic resonance imaging of developmental facial paresis: a spectrum of complex anomalies.
An exome sequencing study of Moebius syndrome including atypical cases reveals an individual with CFEOM3A and a TUBB3 mutation.
A novel homozygous HOXB1 mutation in a Turkish family with hereditary congenital facial paresis.
Homozygous HOXB1 loss-of-function mutation in a large family with hereditary congenital facial paresis.
A new hereditary congenital facial palsy case supports arg5 in HOX-DNA binding domain as possible hot spot for mutations.