Compound heterozygous mutations in the IFT140 gene cause Opitz trigonocephaly C syndrome in a patient with typical features of a ciliopathy von Peña‐Padilla, C., Marshall, C.R., Walker, S., Scherer, S.W., Tavares‐Macías, G., Razo‐Jiménez, G., Bobadilla‐Morales, L., Acosta‐Fernández, E., Corona‐Rivera, A., Mendoza‐Londono, R., Corona‐Rivera, J. R.

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