De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith–Magenis syndromeSarah H. Elsea, Francesco Vetrini, Shane McKee et al.|Genome Medicine|2019Cited by 48
<i>IRF6</i> Screening of Syndromic and a priori Non-Syndromic Cleft Lip and Palate Patients: Identification of a New Type of Minor VWS SignLaurence Desmyter, Miikka Vikkula, Yves Sznajer et al.|Molecular Syndromology|2010Cited by 29
Correction to: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith–Magenis syndromeSarah H. Elsea, Francesco Vetrini, Shane McKee et al.|Genome Medicine|2019Cited by 2
Correction to: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith-Magenis syndromeFrancesco Vetrini, Jennifer E. Posey, Shane McKee et al.|PMC|2019Cited by 1